Canonical Allele Identifier: CA1580179032
Gene:

Linked Data

dbSNP Id: rs1749024373

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002728C>T , CM000667.2:g.126002728C>T GRCh38
NC_000005.9:g.125338421C>T , CM000667.1:g.125338421C>T GRCh37
NC_000005.8:g.125366320C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3612G>A
XR_948738.1:n.497+5812G>A