Canonical Allele Identifier: CA1064137061
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1718660001
gnomAD v3: 4-73404256-G-A
gnomAD v4: 4-73404256-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404256G>A , CM000666.2:g.73404256G>A GRCh38
NC_000004.11:g.74269973G>A , CM000666.1:g.74269973G>A GRCh37
NC_000004.10:g.74488837G>A NCBI36
NG_009291.1:g.5002G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-72G>A ENSP00000295897.4:n.-72G>A
ENST00000441319.5:c.48-113G>A ENSP00000392541.1:n.48-113G>A
ENST00000621628.4:c.-72G>A ENSP00000480485.1:n.-72G>A
NM_000477.5:c.-72G>A NP_000468.1:n.-72G>A
NM_000477.6:c.-72G>A NP_000468.1:n.-72G>A