Canonical Allele Identifier: CA14112022
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs11856995

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782414T>C , CM000677.2:g.95782414T>C GRCh38
NC_000015.9:g.96325643T>C , CM000677.1:g.96325643T>C GRCh37
NC_000015.8:g.94126647T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932654.1:n.148-42775T>C