Canonical Allele Identifier: CA2469949907
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7680780C= , CM000686.2:g.7680780C= GRCh38
NC_000024.9:g.7548821C= , CM000686.1:g.7548821C= GRCh37
NC_000024.8:g.7608821C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439805.1:n.532C=