Canonical Allele Identifier: CA2959566

Gene: ALB

Linked Data

• dbSNP Id: rs11538215
• ExAC: 4:74280870 T / A
• gnomAD v2: 4-74280870-T-A
• gnomAD v3: 4-73415153-T-A
• gnomAD v4: 4-73415153-T-A
• MyVariant Identifiers: chr4:g.74280870T>A (hg19) ; chr4:g.73415153T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415153T>A , CM000666.2:g.73415153T>A	GRCh38
NC_000004.11:g.74280870T>A , CM000666.1:g.74280870T>A	GRCh37
NC_000004.10:g.74499734T>A	NCBI36
NG_009291.1:g.15899T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1177T>A MANE Select	ENSP00000295897.4:p.Cys393Ser
ENST00000295897.8:c.1177T>A	ENSP00000295897.4:p.Cys393Ser
ENST00000401494.7:c.832T>A	ENSP00000384695.3:p.Cys278Ser
ENST00000415165.6:c.601T>A	ENSP00000401820.2:p.Cys201Ser
ENST00000476441.6:c.*456T>A	ENSP00000423727.1:n.*456T>A
ENST00000484992.1:n.497T>A
ENST00000503124.5:c.727T>A	ENSP00000421027.1:p.Cys243Ser
ENST00000504043.1:n.180T>A
ENST00000505649.5:n.863T>A
ENST00000509063.5:c.1177T>A	ENSP00000422784.1:p.Cys393Ser
ENST00000511370.1:c.710T>A
ENST00000621085.4:c.538T>A	ENSP00000483421.1:p.Cys180Ser
ENST00000621628.4:c.538T>A	ENSP00000480485.1:p.Cys180Ser
NM_000477.5:c.1177T>A	NP_000468.1:p.Cys393Ser
NM_000477.6:c.1177T>A	NP_000468.1:p.Cys393Ser
NM_000477.7:c.1177T>A MANE Select	NP_000468.1:p.Cys393Ser