Canonical Allele Identifier: CA99700618

Gene: ALB

Linked Data

• dbSNP Id: rs1032843657
• gnomAD v2: 4-74274475-T-G
• gnomAD v3: 4-73408758-T-G
• gnomAD v4: 4-73408758-T-G
• MyVariant Identifiers: chr4:g.74274475T>G (hg19) ; chr4:g.73408758T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408758T>G , CM000666.2:g.73408758T>G	GRCh38
NC_000004.11:g.74274475T>G , CM000666.1:g.74274475T>G	GRCh37
NC_000004.10:g.74493339T>G	NCBI36
NG_009291.1:g.9504T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.435T>G MANE Select	ENSP00000295897.4:p.Asp145Glu
ENST00000295897.8:c.435T>G	ENSP00000295897.4:p.Asp145Glu
ENST00000401494.7:c.138-597T>G	ENSP00000384695.3:n.138-597T>G
ENST00000415165.6:c.138-3238T>G	ENSP00000401820.2:n.138-3238T>G
ENST00000441319.5:c.441T>G	ENSP00000392541.1:p.Asp147Glu
ENST00000476441.6:c.80-597T>G	ENSP00000423727.1:n.80-597T>G
ENST00000503124.5:c.33-597T>G	ENSP00000421027.1:n.33-597T>G
ENST00000505649.5:n.121T>G
ENST00000509063.5:c.435T>G	ENSP00000422784.1:p.Asp145Glu
ENST00000510166.5:n.471T>G
ENST00000514786.1:n.404T>G
ENST00000515133.5:n.476T>G
ENST00000621085.4:c.435T>G	ENSP00000483421.1:p.Asp145Glu
ENST00000621628.4:c.435T>G	ENSP00000480485.1:p.Asp145Glu
NM_000477.5:c.435T>G	NP_000468.1:p.Asp145Glu
NM_000477.6:c.435T>G	NP_000468.1:p.Asp145Glu
NM_000477.7:c.435T>G MANE Select	NP_000468.1:p.Asp145Glu