Canonical Allele Identifier: CA439799182

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74274487T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408770T>G , CM000666.2:g.73408770T>G	GRCh38
NC_000004.11:g.74274487T>G , CM000666.1:g.74274487T>G	GRCh37
NC_000004.10:g.74493351T>G	NCBI36
NG_009291.1:g.9516T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.447T>G MANE Select	ENSP00000295897.4:p.Thr149=
ENST00000295897.8:c.447T>G	ENSP00000295897.4:p.Thr149=
ENST00000401494.7:c.138-585T>G	ENSP00000384695.3:n.138-585T>G
ENST00000415165.6:c.138-3226T>G	ENSP00000401820.2:n.138-3226T>G
ENST00000441319.5:c.453T>G	ENSP00000392541.1:p.Thr151=
ENST00000476441.6:c.80-585T>G	ENSP00000423727.1:n.80-585T>G
ENST00000503124.5:c.33-585T>G	ENSP00000421027.1:n.33-585T>G
ENST00000505649.5:n.133T>G
ENST00000509063.5:c.447T>G	ENSP00000422784.1:p.Thr149=
ENST00000510166.5:n.483T>G
ENST00000514786.1:n.416T>G
ENST00000515133.5:n.488T>G
ENST00000621085.4:c.447T>G	ENSP00000483421.1:p.Thr149=
ENST00000621628.4:c.447T>G	ENSP00000480485.1:p.Thr149=
NM_000477.5:c.447T>G	NP_000468.1:p.Thr149=
NM_000477.6:c.447T>G	NP_000468.1:p.Thr149=
NM_000477.7:c.447T>G MANE Select	NP_000468.1:p.Thr149=