Canonical Allele Identifier: CA552304196

Gene: ALB

Linked Data

• dbSNP Id: rs1377812129
• gnomAD v2: 4-74269932-A-G
• gnomAD v3: 4-73404215-A-G
• gnomAD v4: 4-73404215-A-G
• MyVariant Identifiers: chr4:g.74269932A>G (hg19) ; chr4:g.73404215A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404215A>G , CM000666.2:g.73404215A>G	GRCh38
NC_000004.11:g.74269932A>G , CM000666.1:g.74269932A>G	GRCh37
NC_000004.10:g.74488796A>G	NCBI36
NG_009291.1:g.4961A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000441319.5:c.48-154A>G	ENSP00000392541.1:n.48-154A>G