Canonical Allele Identifier: CA2610262436

Gene:

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762612C>T , CM000672.2:g.94762612C>T	GRCh38
NC_000010.10:g.96522369C>T , CM000672.1:g.96522369C>T	GRCh37
NC_000010.9:g.96512359C>T	NCBI36
NG_008384.2:g.4907C>T
NG_008384.3:g.4932C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464755.1:c.932-12446C>T	ENSP00000483243.1:n.932-12446C>T