Canonical Allele Identifier: CA11076650
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs13015714

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102355405G>T , CM000664.2:g.102355405G>T GRCh38
NC_000002.11:g.102971865G>T , CM000664.1:g.102971865G>T GRCh37
NC_000002.10:g.102338297G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000410040.5:c.-28-7228G>T ENSP00000386663.1:p.=