Canonical Allele Identifier: CA2510899744
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8606120C>T , CM000686.2:g.8606120C>T GRCh38
NC_000024.9:g.8474161C>T , CM000686.1:g.8474161C>T GRCh37
NC_000024.8:g.8534161C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000624507.1:c.53-1089G>A ENSP00000485522.1:n.53-1089G>A
ENST00000624593.1:c.92+16732G>A ENSP00000485106.1:n.92+16732G>A