Canonical Allele Identifier: CA439801004

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285341C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419624C>G , CM000666.2:g.73419624C>G	GRCh38
NC_000004.11:g.74285341C>G , CM000666.1:g.74285341C>G	GRCh37
NC_000004.10:g.74504205C>G	NCBI36
NG_009291.1:g.20370C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1770C>G MANE Select	ENSP00000295897.4:p.Thr590=
ENST00000295897.8:c.1770C>G	ENSP00000295897.4:p.Thr590=
ENST00000401494.7:c.1425C>G	ENSP00000384695.3:p.Thr475=
ENST00000415165.6:c.1194C>G	ENSP00000401820.2:p.Thr398=
ENST00000476441.6:c.*1049C>G	ENSP00000423727.1:n.*1049C>G
ENST00000495173.1:n.78C>G
ENST00000503124.5:c.1320C>G	ENSP00000421027.1:p.Thr440=
ENST00000505649.5:n.1317C>G
ENST00000508932.5:n.175+169C>G
ENST00000509063.5:c.1770C>G	ENSP00000422784.1:p.Thr590=
ENST00000511370.1:c.1303C>G
ENST00000621085.4:c.1131C>G	ENSP00000483421.1:p.Thr377=
ENST00000621628.4:c.1131C>G	ENSP00000480485.1:p.Thr377=
NM_000477.5:c.1770C>G	NP_000468.1:p.Thr590=
NM_000477.6:c.1770C>G	NP_000468.1:p.Thr590=
NM_000477.7:c.1770C>G MANE Select	NP_000468.1:p.Thr590=