Canonical Allele Identifier: CA439799493

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275159A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409442A>G , CM000666.2:g.73409442A>G	GRCh38
NC_000004.11:g.74275159A>G , CM000666.1:g.74275159A>G	GRCh37
NC_000004.10:g.74494023A>G	NCBI36
NG_009291.1:g.10188A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.570A>G MANE Select	ENSP00000295897.4:p.Thr190=
ENST00000295897.8:c.570A>G	ENSP00000295897.4:p.Thr190=
ENST00000401494.7:c.225A>G	ENSP00000384695.3:p.Thr75=
ENST00000415165.6:c.138-2554A>G	ENSP00000401820.2:n.138-2554A>G
ENST00000441319.5:c.576A>G	ENSP00000392541.1:p.Thr192=
ENST00000476441.6:c.167A>G	ENSP00000423727.1:p.Gln56Arg
ENST00000503124.5:c.120A>G	ENSP00000421027.1:p.Thr40=
ENST00000505649.5:n.256A>G
ENST00000509063.5:c.570A>G	ENSP00000422784.1:p.Thr190=
ENST00000511370.1:c.103A>G
ENST00000514786.1:n.539A>G
ENST00000621085.4:c.490+80A>G	ENSP00000483421.1:n.490+80A>G
ENST00000621628.4:c.486+366A>G	ENSP00000480485.1:n.486+366A>G
NM_000477.5:c.570A>G	NP_000468.1:p.Thr190=
NM_000477.6:c.570A>G	NP_000468.1:p.Thr190=
NM_000477.7:c.570A>G MANE Select	NP_000468.1:p.Thr190=