Linked Data
ClinVar Variation Id:
2820259
ClinVar RCV Id:
RCV003747097
gnomAD v4:
19-1401405-G-T
MyVariant Identifiers:
chr19:g.1401404G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1401405G>T , CM000681.2:g.1401405G>T | GRCh38 |
| NC_000019.9:g.1401404G>T , CM000681.1:g.1401404G>T | GRCh37 |
| NC_000019.8:g.1352404G>T | NCBI36 |
| NG_009785.1:g.5149C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252288.8:c.72C>A MANE Select | ENSP00000252288.1:p.Pro24= | |
| ENST00000447102.8:c.72C>A | ENSP00000403536.2:p.Pro24= | |
| ENST00000640762.1:c.72C>A | ENSP00000492031.1:p.Pro24= | |
| ENST00000252288.6:c.72C>A | ENSP00000252288.1:p.Pro24= | |
| ENST00000447102.7:c.72C>A | ENSP00000403536.2:p.Pro24= | |
| NM_000156.5:c.72C>A | NP_000147.1:p.Pro24= | |
| NM_138924.2:c.72C>A | NP_620279.1:p.Pro24= | |
| NM_000156.6:c.72C>A MANE Select | NP_000147.1:p.Pro24= | |
| NM_138924.3:c.72C>A | NP_620279.1:p.Pro24= |