Canonical Allele Identifier: CA439800284

Gene: ALB

Linked Data

• dbSNP Id: rs1330676658
• gnomAD v4: 4-73415080-G-A
• MyVariant Identifiers: chr4:g.74280797G>A (hg19) ; chr4:g.73415080G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415080G>A , CM000666.2:g.73415080G>A	GRCh38
NC_000004.11:g.74280797G>A , CM000666.1:g.74280797G>A	GRCh37
NC_000004.10:g.74499661G>A	NCBI36
NG_009291.1:g.15826G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1104G>A MANE Select	ENSP00000295897.4:p.Val368=
ENST00000295897.8:c.1104G>A	ENSP00000295897.4:p.Val368=
ENST00000401494.7:c.759G>A	ENSP00000384695.3:p.Val253=
ENST00000415165.6:c.528G>A	ENSP00000401820.2:p.Val176=
ENST00000476441.6:c.*383G>A	ENSP00000423727.1:n.*383G>A
ENST00000484992.1:n.424G>A
ENST00000503124.5:c.654G>A	ENSP00000421027.1:p.Val218=
ENST00000504043.1:n.107G>A
ENST00000505649.5:n.790G>A
ENST00000509063.5:c.1104G>A	ENSP00000422784.1:p.Val368=
ENST00000511370.1:c.637G>A
ENST00000621085.4:c.491-26G>A	ENSP00000483421.1:n.491-26G>A
ENST00000621628.4:c.487-22G>A	ENSP00000480485.1:n.487-22G>A
NM_000477.5:c.1104G>A	NP_000468.1:p.Val368=
NM_000477.6:c.1104G>A	NP_000468.1:p.Val368=
NM_000477.7:c.1104G>A MANE Select	NP_000468.1:p.Val368=