Canonical Allele Identifier: CA1580179008
Gene:

Linked Data

dbSNP Id: rs1749023749

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002684A>G , CM000667.2:g.126002684A>G GRCh38
NC_000005.9:g.125338377A>G , CM000667.1:g.125338377A>G GRCh37
NC_000005.8:g.125366276A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3656T>C
XR_948738.1:n.497+5856T>C