Canonical Allele Identifier: CA1580179021
Gene:

Linked Data

dbSNP Id: rs1749024050

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002701C>T , CM000667.2:g.126002701C>T GRCh38
NC_000005.9:g.125338394C>T , CM000667.1:g.125338394C>T GRCh37
NC_000005.8:g.125366293C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3639G>A
XR_948738.1:n.497+5839G>A