Canonical Allele Identifier: CA2670936421
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404277-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404277T>A , CM000666.2:g.73404277T>A GRCh38
NC_000004.11:g.74269994T>A , CM000666.1:g.74269994T>A GRCh37
NC_000004.10:g.74488858T>A NCBI36
NG_009291.1:g.5023T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-51T>A ENSP00000295897.4:n.-51T>A
ENST00000441319.5:c.48-92T>A ENSP00000392541.1:n.48-92T>A
ENST00000621628.4:c.-51T>A ENSP00000480485.1:n.-51T>A
NM_000477.5:c.-51T>A NP_000468.1:n.-51T>A
NM_000477.6:c.-51T>A NP_000468.1:n.-51T>A