Canonical Allele Identifier: CA798282571
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1174816129
gnomAD v4: 4-73404117-A-G
MyVariant Identifiers: chr4:g.74269834A>G (hg19) chr4:g.73404117A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404117A>G , CM000666.2:g.73404117A>G GRCh38
NC_000004.11:g.74269834A>G , CM000666.1:g.74269834A>G GRCh37
NC_000004.10:g.74488698A>G NCBI36
NG_009291.1:g.4863A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-252A>G ENSP00000392541.1:n.48-252A>G
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