Canonical Allele Identifier: CA813238967
Gene:

Linked Data

dbSNP Id: rs915200425

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.66487824G>C , CM000667.2:g.66487824G>C GRCh38
NC_000005.9:g.65783652G>C , CM000667.1:g.65783652G>C GRCh37
NC_000005.8:g.65819408G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948381.1:n.649-49012G>C