Canonical Allele Identifier: CA798282605

Gene: ALB

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404178T>C , CM000666.2:g.73404178T>C	GRCh38
NC_000004.11:g.74269895T>C , CM000666.1:g.74269895T>C	GRCh37
NC_000004.10:g.74488759T>C	NCBI36
NG_009291.1:g.4924T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000441319.5:c.48-191T>C	ENSP00000392541.1:n.48-191T>C