Canonical Allele Identifier: CA595318354
Gene:

Linked Data

dbSNP Id: rs1468374524

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762527G>T , CM000672.2:g.94762527G>T GRCh38
NC_000010.10:g.96522284G>T , CM000672.1:g.96522284G>T GRCh37
NC_000010.9:g.96512274G>T NCBI36
NG_008384.2:g.4822G>T
NG_008384.3:g.4847G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000464755.1:c.932-12531G>T ENSP00000483243.1:n.932-12531G>T