Canonical Allele Identifier: CA1929213301
Gene:

Linked Data

dbSNP Id: rs1848182091

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762487G>A , CM000672.2:g.94762487G>A GRCh38
NC_000010.10:g.96522244G>A , CM000672.1:g.96522244G>A GRCh37
NC_000010.9:g.96512234G>A NCBI36
NG_008384.2:g.4782G>A
NG_008384.3:g.4807G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12571G>A ENSP00000483243.1:n.932-12571G>A