Canonical Allele Identifier: CA357236373

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74274318T>G (hg19) ; chr4:g.73408601T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408601T>G , CM000666.2:g.73408601T>G	GRCh38
NC_000004.11:g.74274318T>G , CM000666.1:g.74274318T>G	GRCh37
NC_000004.10:g.74493182T>G	NCBI36
NG_009291.1:g.9347T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.278T>G MANE Select	ENSP00000295897.4:p.Leu93Arg
ENST00000295897.8:c.278T>G	ENSP00000295897.4:p.Leu93Arg
ENST00000401494.7:c.138-754T>G	ENSP00000384695.3:n.138-754T>G
ENST00000415165.6:c.138-3395T>G	ENSP00000401820.2:n.138-3395T>G
ENST00000441319.5:c.284T>G	ENSP00000392541.1:p.Leu95Arg
ENST00000476441.6:c.80-754T>G	ENSP00000423727.1:n.80-754T>G
ENST00000503124.5:c.33-754T>G	ENSP00000421027.1:n.33-754T>G
ENST00000509063.5:c.278T>G	ENSP00000422784.1:p.Leu93Arg
ENST00000510166.5:n.314T>G
ENST00000514786.1:n.247T>G
ENST00000515133.5:n.319T>G
ENST00000621085.4:c.278T>G	ENSP00000483421.1:p.Leu93Arg
ENST00000621628.4:c.278T>G	ENSP00000480485.1:p.Leu93Arg
NM_000477.5:c.278T>G	NP_000468.1:p.Leu93Arg
NM_000477.6:c.278T>G	NP_000468.1:p.Leu93Arg
NM_000477.7:c.278T>G MANE Select	NP_000468.1:p.Leu93Arg