Canonical Allele Identifier: CA357240614
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73413478A>G , CM000666.2:g.73413478A>G GRCh38
NC_000004.11:g.74279195A>G , CM000666.1:g.74279195A>G GRCh37
NC_000004.10:g.74498059A>G NCBI36
NG_009291.1:g.14224A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.902A>G MANE Select ENSP00000295897.4:p.Glu301Gly
ENST00000295897.8:c.902A>G ENSP00000295897.4:p.Glu301Gly
ENST00000401494.7:c.557A>G ENSP00000384695.3:p.Glu186Gly
ENST00000415165.6:c.326A>G ENSP00000401820.2:p.Glu109Gly
ENST00000476441.6:c.*181A>G ENSP00000423727.1:n.*181A>G
ENST00000484992.1:n.222A>G
ENST00000503124.5:c.452A>G ENSP00000421027.1:p.Glu151Gly
ENST00000505649.5:n.588A>G
ENST00000509063.5:c.902A>G ENSP00000422784.1:p.Glu301Gly
ENST00000511370.1:c.435A>G
ENST00000621085.4:c.491-1628A>G ENSP00000483421.1:n.491-1628A>G
ENST00000621628.4:c.487-1624A>G ENSP00000480485.1:n.487-1624A>G
NM_000477.5:c.902A>G NP_000468.1:p.Glu301Gly
NM_000477.6:c.902A>G NP_000468.1:p.Glu301Gly
NM_000477.7:c.902A>G MANE Select NP_000468.1:p.Glu301Gly