Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23419566T>C , CM000676.2:g.23419566T>C | GRCh38 |
| NC_000014.8:g.23888775T>C , CM000676.1:g.23888775T>C | GRCh37 |
| NC_000014.7:g.22958615T>C | NCBI36 |
| NG_007884.1:g.21096A>G , LRG_384:g.21096A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000257.4:c.3770A>G MANE Select | NP_000248.2:p.Asn1257Ser |
| ENST00000355349.4:c.3770A>G MANE Select | ENSP00000347507.3:p.Asn1257Ser |
| NM_000257.3:c.3770A>G | NP_000248.2:p.Asn1257Ser |
| ENST00000355349.3:c.3770A>G | ENSP00000347507.3:p.Asn1257Ser |
| XM_017021340.1:c.3770A>G | XP_016876829.1:p.Asn1257Ser |