Canonical Allele Identifier: CA2467802761
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.641065C= , CM000686.2:g.641065C= GRCh38
NC_000024.9:g.551800C= , CM000686.1:g.551800C= GRCh37
NC_000024.8:g.521800C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000711141.1:c.611C= ENSP00000518639.1:p.Ala204=
ENST00000711142.1:c.611C= ENSP00000518640.1:p.Ala204=
ENST00000711143.1:c.611C= ENSP00000518641.1:p.Ala204=
ENST00000711145.1:c.611C= ENSP00000518642.1:p.Ala204=