Canonical Allele Identifier: CA2959551

Gene: ALB

Linked Data

• dbSNP Id: rs778539083
• ExAC: 4:74280795 G / A
• gnomAD v2: 4-74280795-G-A
• gnomAD v4: 4-73415078-G-A
• MyVariant Identifiers: chr4:g.74280795G>A (hg19) ; chr4:g.73415078G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415078G>A , CM000666.2:g.73415078G>A	GRCh38
NC_000004.11:g.74280795G>A , CM000666.1:g.74280795G>A	GRCh37
NC_000004.10:g.74499659G>A	NCBI36
NG_009291.1:g.15824G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1102G>A MANE Select	ENSP00000295897.4:p.Val368Met
ENST00000295897.8:c.1102G>A	ENSP00000295897.4:p.Val368Met
ENST00000401494.7:c.757G>A	ENSP00000384695.3:p.Val253Met
ENST00000415165.6:c.526G>A	ENSP00000401820.2:p.Val176Met
ENST00000476441.6:c.*381G>A	ENSP00000423727.1:n.*381G>A
ENST00000484992.1:n.422G>A
ENST00000503124.5:c.652G>A	ENSP00000421027.1:p.Val218Met
ENST00000504043.1:n.105G>A
ENST00000505649.5:n.788G>A
ENST00000509063.5:c.1102G>A	ENSP00000422784.1:p.Val368Met
ENST00000511370.1:c.635G>A
ENST00000621085.4:c.491-28G>A	ENSP00000483421.1:n.491-28G>A
ENST00000621628.4:c.487-24G>A	ENSP00000480485.1:n.487-24G>A
NM_000477.5:c.1102G>A	NP_000468.1:p.Val368Met
NM_000477.6:c.1102G>A	NP_000468.1:p.Val368Met
NM_000477.7:c.1102G>A MANE Select	NP_000468.1:p.Val368Met