Canonical Allele Identifier: CA99696251

Gene: ALB

Linked Data

• dbSNP Id: rs907562413
• gnomAD v2: 4-74269954-A-C
• gnomAD v3: 4-73404237-A-C
• gnomAD v4: 4-73404237-A-C
• MyVariant Identifiers: chr4:g.74269954A>C (hg19) ; chr4:g.73404237A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404237A>C , CM000666.2:g.73404237A>C	GRCh38
NC_000004.11:g.74269954A>C , CM000666.1:g.74269954A>C	GRCh37
NC_000004.10:g.74488818A>C	NCBI36
NG_009291.1:g.4983A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000441319.5:c.48-132A>C	ENSP00000392541.1:n.48-132A>C