Canonical Allele Identifier: CA2610262439

Gene:

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762618A>G , CM000672.2:g.94762618A>G	GRCh38
NC_000010.10:g.96522375A>G , CM000672.1:g.96522375A>G	GRCh37
NC_000010.9:g.96512365A>G	NCBI36
NG_008384.2:g.4913A>G
NG_008384.3:g.4938A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464755.1:c.932-12440A>G	ENSP00000483243.1:n.932-12440A>G