Canonical Allele Identifier: CA357235912

Gene: ALB

Linked Data

• dbSNP Id: rs1164942407
• gnomAD v2: 4-74272447-A-T
• gnomAD v3: 4-73406730-A-T
• gnomAD v4: 4-73406730-A-T
• MyVariant Identifiers: chr4:g.74272447A>T (hg19) ; chr4:g.73406730A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406730A>T , CM000666.2:g.73406730A>T	GRCh38
NC_000004.11:g.74272447A>T , CM000666.1:g.74272447A>T	GRCh37
NC_000004.10:g.74491311A>T	NCBI36
NG_009291.1:g.7476A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.239A>T MANE Select	ENSP00000295897.4:p.Asp80Val
ENST00000295897.8:c.239A>T	ENSP00000295897.4:p.Asp80Val
ENST00000401494.7:c.137+1557A>T	ENSP00000384695.3:n.137+1557A>T
ENST00000415165.6:c.137+1557A>T	ENSP00000401820.2:n.137+1557A>T
ENST00000441319.5:c.245A>T	ENSP00000392541.1:p.Asp82Val
ENST00000476441.6:c.79+2324A>T	ENSP00000423727.1:n.79+2324A>T
ENST00000503124.5:c.1A>T	ENSP00000421027.1:p.Met1Leu
ENST00000509063.5:c.239A>T	ENSP00000422784.1:p.Asp80Val
ENST00000510166.5:n.275A>T
ENST00000514786.1:n.208A>T
ENST00000515133.5:n.280A>T
ENST00000621085.4:c.239A>T	ENSP00000483421.1:p.Asp80Val
ENST00000621628.4:c.239A>T	ENSP00000480485.1:p.Asp80Val
NM_000477.5:c.239A>T	NP_000468.1:p.Asp80Val
NM_000477.6:c.239A>T	NP_000468.1:p.Asp80Val
NM_000477.7:c.239A>T MANE Select	NP_000468.1:p.Asp80Val