Canonical Allele Identifier: CA2614496195

Gene:

Linked Data

• gnomAD v4: 11-66510605-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66510605C>T , CM000673.2:g.66510605C>T	GRCh38
NC_000011.9:g.66278076C>T , CM000673.1:g.66278076C>T	GRCh37
NC_000011.8:g.66034652C>T	NCBI36
NG_009093.1:g.4958C>T
NG_032068.1:g.35197C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419755.3:c.159-408C>T	ENSP00000398526.3:n.159-408C>T