Canonical Allele Identifier: CA803406395
Gene:

Linked Data

dbSNP Id: rs1373037928

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002798G>C , CM000667.2:g.126002798G>C GRCh38
NC_000005.9:g.125338491G>C , CM000667.1:g.125338491G>C GRCh37
NC_000005.8:g.125366390G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3542C>G
XR_948738.1:n.497+5742C>G