Canonical Allele Identifier: CA357236068

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74272464T>G (hg19) ; chr4:g.73406747T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406747T>G , CM000666.2:g.73406747T>G	GRCh38
NC_000004.11:g.74272464T>G , CM000666.1:g.74272464T>G	GRCh37
NC_000004.10:g.74491328T>G	NCBI36
NG_009291.1:g.7493T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.256T>G MANE Select	ENSP00000295897.4:p.Cys86Gly
ENST00000295897.8:c.256T>G	ENSP00000295897.4:p.Cys86Gly
ENST00000401494.7:c.137+1574T>G	ENSP00000384695.3:n.137+1574T>G
ENST00000415165.6:c.137+1574T>G	ENSP00000401820.2:n.137+1574T>G
ENST00000441319.5:c.262T>G	ENSP00000392541.1:p.Cys88Gly
ENST00000476441.6:c.79+2341T>G	ENSP00000423727.1:n.79+2341T>G
ENST00000503124.5:c.18T>G	ENSP00000421027.1:p.Ile6Met
ENST00000509063.5:c.256T>G	ENSP00000422784.1:p.Cys86Gly
ENST00000510166.5:n.292T>G
ENST00000514786.1:n.225T>G
ENST00000515133.5:n.297T>G
ENST00000621085.4:c.256T>G	ENSP00000483421.1:p.Cys86Gly
ENST00000621628.4:c.256T>G	ENSP00000480485.1:p.Cys86Gly
NM_000477.5:c.256T>G	NP_000468.1:p.Cys86Gly
NM_000477.6:c.256T>G	NP_000468.1:p.Cys86Gly
NM_000477.7:c.256T>G MANE Select	NP_000468.1:p.Cys86Gly