Canonical Allele Identifier: CA127888
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 18190
ClinVar RCV Id: RCV000019831
dbSNP Id: rs75522063

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73408750G>A , CM000666.2:g.73408750G>A GRCh38
NC_000004.11:g.74274467G>A , CM000666.1:g.74274467G>A GRCh37
NC_000004.10:g.74493331G>A NCBI36
NG_009291.1:g.9496G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.427G>A MANE Select ENSP00000295897.4:p.Glu143Lys
ENST00000295897.8:c.427G>A ENSP00000295897.4:p.Glu143Lys
ENST00000401494.7:c.138-605G>A ENSP00000384695.3:n.138-605G>A
ENST00000415165.6:c.138-3246G>A ENSP00000401820.2:n.138-3246G>A
ENST00000441319.5:c.433G>A ENSP00000392541.1:p.Glu145Lys
ENST00000476441.6:c.80-605G>A ENSP00000423727.1:n.80-605G>A
ENST00000503124.5:c.33-605G>A ENSP00000421027.1:n.33-605G>A
ENST00000505649.5:n.113G>A
ENST00000509063.5:c.427G>A ENSP00000422784.1:p.Glu143Lys
ENST00000510166.5:n.463G>A
ENST00000514786.1:n.396G>A
ENST00000515133.5:n.468G>A
ENST00000621085.4:c.427G>A ENSP00000483421.1:p.Glu143Lys
ENST00000621628.4:c.427G>A ENSP00000480485.1:p.Glu143Lys
NM_000477.5:c.427G>A NP_000468.1:p.Glu143Lys
NM_000477.6:c.427G>A NP_000468.1:p.Glu143Lys
NM_000477.7:c.427G>A MANE Select NP_000468.1:p.Glu143Lys