Canonical Allele Identifier: CA170829

Gene: ALB

Linked Data

• ClinVar Variation Id: 156321
• ClinVar RCV Id: RCV000144405
• dbSNP Id: rs77752336
• MyVariant Identifiers: chr4:g.74274477T>A (hg19) ; chr4:g.73408760T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408760T>A , CM000666.2:g.73408760T>A	GRCh38
NC_000004.11:g.74274477T>A , CM000666.1:g.74274477T>A	GRCh37
NC_000004.10:g.74493341T>A	NCBI36
NG_009291.1:g.9506T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.437T>A MANE Select	ENSP00000295897.4:p.Val146Glu
ENST00000295897.8:c.437T>A	ENSP00000295897.4:p.Val146Glu
ENST00000401494.7:c.138-595T>A	ENSP00000384695.3:n.138-595T>A
ENST00000415165.6:c.138-3236T>A	ENSP00000401820.2:n.138-3236T>A
ENST00000441319.5:c.443T>A	ENSP00000392541.1:p.Val148Glu
ENST00000476441.6:c.80-595T>A	ENSP00000423727.1:n.80-595T>A
ENST00000503124.5:c.33-595T>A	ENSP00000421027.1:n.33-595T>A
ENST00000505649.5:n.123T>A
ENST00000509063.5:c.437T>A	ENSP00000422784.1:p.Val146Glu
ENST00000510166.5:n.473T>A
ENST00000514786.1:n.406T>A
ENST00000515133.5:n.478T>A
ENST00000621085.4:c.437T>A	ENSP00000483421.1:p.Val146Glu
ENST00000621628.4:c.437T>A	ENSP00000480485.1:p.Val146Glu
NM_000477.5:c.437T>A	NP_000468.1:p.Val146Glu
NM_000477.6:c.437T>A	NP_000468.1:p.Val146Glu
NM_000477.7:c.437T>A MANE Select	NP_000468.1:p.Val146Glu