Canonical Allele Identifier: CA210712
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 14012
ClinVar RCV Id: RCV000015050
dbSNP Id: rs41279104

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439680C>T , CM000674.2:g.117439680C>T GRCh38
NC_000012.11:g.117877485C>T , CM000674.1:g.117877485C>T GRCh37
NC_000012.10:g.116361868C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000549189.1:n.470+12021G>A