Canonical Allele Identifier: CA1929213476

Gene:

Linked Data

• dbSNP Id: rs1848184566
• gnomAD v4: 10-94762622-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762622G>A , CM000672.2:g.94762622G>A	GRCh38
NC_000010.10:g.96522379G>A , CM000672.1:g.96522379G>A	GRCh37
NC_000010.9:g.96512369G>A	NCBI36
NG_008384.2:g.4917G>A
NG_008384.3:g.4942G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000464755.1:c.932-12436G>A	ENSP00000483243.1:n.932-12436G>A