Canonical Allele Identifier: CA357241076
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73415048T>G , CM000666.2:g.73415048T>G GRCh38
NC_000004.11:g.74280765T>G , CM000666.1:g.74280765T>G GRCh37
NC_000004.10:g.74499629T>G NCBI36
NG_009291.1:g.15794T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1072T>G MANE Select ENSP00000295897.4:p.Tyr358Asp
ENST00000295897.8:c.1072T>G ENSP00000295897.4:p.Tyr358Asp
ENST00000401494.7:c.727T>G ENSP00000384695.3:p.Tyr243Asp
ENST00000415165.6:c.496T>G ENSP00000401820.2:p.Tyr166Asp
ENST00000476441.6:c.*351T>G ENSP00000423727.1:n.*351T>G
ENST00000484992.1:n.392T>G
ENST00000503124.5:c.622T>G ENSP00000421027.1:p.Tyr208Asp
ENST00000504043.1:n.75T>G
ENST00000505649.5:n.758T>G
ENST00000509063.5:c.1072T>G ENSP00000422784.1:p.Tyr358Asp
ENST00000511370.1:c.605T>G
ENST00000621085.4:c.491-58T>G ENSP00000483421.1:n.491-58T>G
ENST00000621628.4:c.487-54T>G ENSP00000480485.1:n.487-54T>G
NM_000477.5:c.1072T>G NP_000468.1:p.Tyr358Asp
NM_000477.6:c.1072T>G NP_000468.1:p.Tyr358Asp
NM_000477.7:c.1072T>G MANE Select NP_000468.1:p.Tyr358Asp