Canonical Allele Identifier: CA99696159

Gene: ALB

Linked Data

• dbSNP Id: rs948452660
• gnomAD v3: 4-73404123-A-G
• gnomAD v4: 4-73404123-A-G
• MyVariant Identifiers: chr4:g.74269840A>G (hg19) ; chr4:g.73404123A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404123A>G , CM000666.2:g.73404123A>G	GRCh38
NC_000004.11:g.74269840A>G , CM000666.1:g.74269840A>G	GRCh37
NC_000004.10:g.74488704A>G	NCBI36
NG_009291.1:g.4869A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000441319.5:c.48-246A>G	ENSP00000392541.1:n.48-246A>G