Canonical Allele Identifier: CA2670936320
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404122-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404122C>A , CM000666.2:g.73404122C>A GRCh38
NC_000004.11:g.74269839C>A , CM000666.1:g.74269839C>A GRCh37
NC_000004.10:g.74488703C>A NCBI36
NG_009291.1:g.4868C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-247C>A ENSP00000392541.1:n.48-247C>A
Search 100 bp 5'
Search 100 bp 3'