Canonical Allele Identifier: CA2670936362
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404191-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404191C>A , CM000666.2:g.73404191C>A GRCh38
NC_000004.11:g.74269908C>A , CM000666.1:g.74269908C>A GRCh37
NC_000004.10:g.74488772C>A NCBI36
NG_009291.1:g.4937C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-178C>A ENSP00000392541.1:n.48-178C>A