Linked Data
MyVariant Identifiers:
chr1:g.171621250T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171652110T>G , CM000663.2:g.171652110T>G | GRCh38 |
| NC_000001.10:g.171621250T>G , CM000663.1:g.171621250T>G | GRCh37 |
| NC_000001.9:g.169887873T>G | NCBI36 |
| NG_008859.1:g.5524A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.502A>C MANE Select | ENSP00000037502.5:p.Arg168= | |
| ENST00000638471.1:c.130+372A>C | ENSP00000491206.1:n.130+372A>C | |
| ENST00000037502.10:c.502A>C | ENSP00000037502.5:p.Arg168= | |
| ENST00000614688.1:c.502A>C | ENSP00000478680.1:p.Arg168= | |
| NM_000261.1:c.502A>C | NP_000252.1:p.Arg168= | |
| NM_000261.2:c.502A>C MANE Select | NP_000252.1:p.Arg168= |