Canonical Allele Identifier: CA357234415
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404340A>G , CM000666.2:g.73404340A>G GRCh38
NC_000004.11:g.74270057A>G , CM000666.1:g.74270057A>G GRCh37
NC_000004.10:g.74488921A>G NCBI36
NG_009291.1:g.5086A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.13A>G MANE Select ENSP00000295897.4:p.Thr5Ala
ENST00000295897.8:c.13A>G ENSP00000295897.4:p.Thr5Ala
ENST00000401494.7:c.13A>G ENSP00000384695.3:p.Thr5Ala
ENST00000415165.6:c.13A>G ENSP00000401820.2:p.Thr5Ala
ENST00000441319.5:c.48-29A>G ENSP00000392541.1:n.48-29A>G
ENST00000476441.6:c.13A>G ENSP00000423727.1:p.Thr5Ala
ENST00000503124.5:c.-168A>G ENSP00000421027.1:n.-168A>G
ENST00000509063.5:c.13A>G ENSP00000422784.1:p.Thr5Ala
ENST00000510166.5:n.54A>G
ENST00000514786.1:n.48+4A>G
ENST00000515133.5:n.54A>G
ENST00000621085.4:c.13A>G ENSP00000483421.1:p.Thr5Ala
ENST00000621628.4:c.13A>G ENSP00000480485.1:p.Thr5Ala
NM_000477.5:c.13A>G NP_000468.1:p.Thr5Ala
NM_000477.6:c.13A>G NP_000468.1:p.Thr5Ala
NM_000477.7:c.13A>G MANE Select NP_000468.1:p.Thr5Ala