Canonical Allele Identifier: CA2670936395
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404241-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404241T>A , CM000666.2:g.73404241T>A GRCh38
NC_000004.11:g.74269958T>A , CM000666.1:g.74269958T>A GRCh37
NC_000004.10:g.74488822T>A NCBI36
NG_009291.1:g.4987T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-87T>A ENSP00000295897.4:n.-87T>A
ENST00000441319.5:c.48-128T>A ENSP00000392541.1:n.48-128T>A
NM_000477.6:c.-87T>A NP_000468.1:n.-87T>A