Canonical Allele Identifier: CA931367358
Gene:

Linked Data

dbSNP Id: rs1848181813

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762464A>G , CM000672.2:g.94762464A>G GRCh38
NC_000010.10:g.96522221A>G , CM000672.1:g.96522221A>G GRCh37
NC_000010.9:g.96512211A>G NCBI36
NG_008384.2:g.4759A>G
NG_008384.3:g.4784A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12594A>G ENSP00000483243.1:n.932-12594A>G