Canonical Allele Identifier: CA257933329

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24635154A>T , CM000676.2:g.24635154A>T	GRCh38
NC_000014.8:g.25104360A>T , CM000676.1:g.25104360A>T	GRCh37
NC_000014.7:g.24174200A>T	NCBI36
NG_028340.1:g.4073T>A

Transcript Alleles

HGVS	Amino-acid Change
XR_001750665.1:n.549+577A>T