Canonical Allele Identifier: CA99696233

Gene: ALB

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404193G>T , CM000666.2:g.73404193G>T	GRCh38
NC_000004.11:g.74269910G>T , CM000666.1:g.74269910G>T	GRCh37
NC_000004.10:g.74488774G>T	NCBI36
NG_009291.1:g.4939G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000441319.5:c.48-176G>T	ENSP00000392541.1:n.48-176G>T