Canonical Allele Identifier: CA439798765
Gene: ALB HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.74272433A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73406716A>G , CM000666.2:g.73406716A>G GRCh38
NC_000004.11:g.74272433A>G , CM000666.1:g.74272433A>G GRCh37
NC_000004.10:g.74491297A>G NCBI36
NG_009291.1:g.7462A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.225A>G MANE Select ENSP00000295897.4:p.Lys75=
ENST00000295897.8:c.225A>G ENSP00000295897.4:p.Lys75=
ENST00000401494.7:c.137+1543A>G ENSP00000384695.3:n.137+1543A>G
ENST00000415165.6:c.137+1543A>G ENSP00000401820.2:n.137+1543A>G
ENST00000441319.5:c.231A>G ENSP00000392541.1:p.Lys77=
ENST00000476441.6:c.79+2310A>G ENSP00000423727.1:n.79+2310A>G
ENST00000503124.5:c.-14A>G ENSP00000421027.1:n.-14A>G
ENST00000509063.5:c.225A>G ENSP00000422784.1:p.Lys75=
ENST00000510166.5:n.261A>G
ENST00000514786.1:n.194A>G
ENST00000515133.5:n.266A>G
ENST00000621085.4:c.225A>G ENSP00000483421.1:p.Lys75=
ENST00000621628.4:c.225A>G ENSP00000480485.1:p.Lys75=
NM_000477.5:c.225A>G NP_000468.1:p.Lys75=
NM_000477.6:c.225A>G NP_000468.1:p.Lys75=
NM_000477.7:c.225A>G MANE Select NP_000468.1:p.Lys75=