Canonical Allele Identifier: CA170833

Gene: ALB

Linked Data

• ClinVar Variation Id: 156323
• ClinVar RCV Id: RCV000144407
• dbSNP Id: rs76454301
• MyVariant Identifiers: chr4:g.74277713G>A (hg19) ; chr4:g.73411996G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73411996G>A , CM000666.2:g.73411996G>A	GRCh38
NC_000004.11:g.74277713G>A , CM000666.1:g.74277713G>A	GRCh37
NC_000004.10:g.74496577G>A	NCBI36
NG_009291.1:g.12742G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.714G>A MANE Select	ENSP00000295897.4:p.Trp238Ter
ENST00000295897.8:c.714G>A	ENSP00000295897.4:p.Trp238Ter
ENST00000401494.7:c.369G>A	ENSP00000384695.3:p.Trp123Ter
ENST00000415165.6:c.138G>A	ENSP00000401820.2:p.Leu46=
ENST00000476441.6:c.311G>A	ENSP00000423727.1:p.Gly104Glu
ENST00000503124.5:c.264G>A	ENSP00000421027.1:p.Trp88Ter
ENST00000505649.5:n.400G>A
ENST00000507673.1:n.31G>A
ENST00000509063.5:c.714G>A	ENSP00000422784.1:p.Trp238Ter
ENST00000511370.1:c.247G>A
ENST00000621085.4:c.490+2634G>A	ENSP00000483421.1:n.490+2634G>A
ENST00000621628.4:c.486+2920G>A	ENSP00000480485.1:n.486+2920G>A
NM_000477.5:c.714G>A	NP_000468.1:p.Trp238Ter
NM_000477.6:c.714G>A	NP_000468.1:p.Trp238Ter
NM_000477.7:c.714G>A MANE Select	NP_000468.1:p.Trp238Ter