Canonical Allele Identifier: CA2959678
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs762887582
gnomAD v2: 4-74283856-A-T
gnomAD v4: 4-73418139-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73418139A>T , CM000666.2:g.73418139A>T GRCh38
NC_000004.11:g.74283856A>T , CM000666.1:g.74283856A>T GRCh37
NC_000004.10:g.74502720A>T NCBI36
NG_009291.1:g.18885A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1480A>T MANE Select ENSP00000295897.4:p.Ser494Cys
ENST00000295897.8:c.1480A>T ENSP00000295897.4:p.Ser494Cys
ENST00000401494.7:c.1135A>T ENSP00000384695.3:p.Ser379Cys
ENST00000415165.6:c.904A>T ENSP00000401820.2:p.Ser302Cys
ENST00000476441.6:c.*759A>T ENSP00000423727.1:n.*759A>T
ENST00000486939.1:n.134A>T
ENST00000503124.5:c.1030A>T ENSP00000421027.1:p.Ser344Cys
ENST00000505649.5:n.1027A>T
ENST00000509063.5:c.1480A>T ENSP00000422784.1:p.Ser494Cys
ENST00000511370.1:c.1013A>T
ENST00000621085.4:c.841A>T ENSP00000483421.1:p.Ser281Cys
ENST00000621628.4:c.841A>T ENSP00000480485.1:p.Ser281Cys
NM_000477.5:c.1480A>T NP_000468.1:p.Ser494Cys
NM_000477.6:c.1480A>T NP_000468.1:p.Ser494Cys
NM_000477.7:c.1480A>T MANE Select NP_000468.1:p.Ser494Cys