Canonical Allele Identifier: CA357238079

Gene: ALB

Linked Data

• dbSNP Id: rs1232971594
• gnomAD v2: 4-74275098-A-G
• gnomAD v4: 4-73409381-A-G
• MyVariant Identifiers: chr4:g.74275098A>G (hg19) ; chr4:g.73409381A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409381A>G , CM000666.2:g.73409381A>G	GRCh38
NC_000004.11:g.74275098A>G , CM000666.1:g.74275098A>G	GRCh37
NC_000004.10:g.74493962A>G	NCBI36
NG_009291.1:g.10127A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.509A>G MANE Select	ENSP00000295897.4:p.His170Arg
ENST00000295897.8:c.509A>G	ENSP00000295897.4:p.His170Arg
ENST00000401494.7:c.164A>G	ENSP00000384695.3:p.His55Arg
ENST00000415165.6:c.138-2615A>G	ENSP00000401820.2:n.138-2615A>G
ENST00000441319.5:c.515A>G	ENSP00000392541.1:p.His172Arg
ENST00000476441.6:c.106A>G	ENSP00000423727.1:p.Ile36Val
ENST00000503124.5:c.59A>G	ENSP00000421027.1:p.His20Arg
ENST00000505649.5:n.195A>G
ENST00000509063.5:c.509A>G	ENSP00000422784.1:p.His170Arg
ENST00000511370.1:c.42A>G
ENST00000514786.1:n.478A>G
ENST00000621085.4:c.490+19A>G	ENSP00000483421.1:n.490+19A>G
ENST00000621628.4:c.486+305A>G	ENSP00000480485.1:n.486+305A>G
NM_000477.5:c.509A>G	NP_000468.1:p.His170Arg
NM_000477.6:c.509A>G	NP_000468.1:p.His170Arg
NM_000477.7:c.509A>G MANE Select	NP_000468.1:p.His170Arg