Canonical Allele Identifier: CA357244452

Gene: ALB

Linked Data

• dbSNP Id: rs80259813
• MyVariant Identifiers: chr4:g.74283883G>T (hg19) ; chr4:g.73418166G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418166G>T , CM000666.2:g.73418166G>T	GRCh38
NC_000004.11:g.74283883G>T , CM000666.1:g.74283883G>T	GRCh37
NC_000004.10:g.74502747G>T	NCBI36
NG_009291.1:g.18912G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1507G>T MANE Select	ENSP00000295897.4:p.Glu503Ter
ENST00000295897.8:c.1507G>T	ENSP00000295897.4:p.Glu503Ter
ENST00000401494.7:c.1162G>T	ENSP00000384695.3:p.Glu388Ter
ENST00000415165.6:c.931G>T	ENSP00000401820.2:p.Glu311Ter
ENST00000476441.6:c.*786G>T	ENSP00000423727.1:n.*786G>T
ENST00000486939.1:n.161G>T
ENST00000503124.5:c.1057G>T	ENSP00000421027.1:p.Glu353Ter
ENST00000505649.5:n.1054G>T
ENST00000509063.5:c.1507G>T	ENSP00000422784.1:p.Glu503Ter
ENST00000511370.1:c.1040G>T
ENST00000621085.4:c.868G>T	ENSP00000483421.1:p.Glu290Ter
ENST00000621628.4:c.868G>T	ENSP00000480485.1:p.Glu290Ter
NM_000477.5:c.1507G>T	NP_000468.1:p.Glu503Ter
NM_000477.6:c.1507G>T	NP_000468.1:p.Glu503Ter
NM_000477.7:c.1507G>T MANE Select	NP_000468.1:p.Glu503Ter