Canonical Allele Identifier: CA127945

Gene: ALB

Linked Data

• ClinVar Variation Id: 18221
• ClinVar RCV Id: RCV000019882
• dbSNP Id: rs80095457
• MyVariant Identifiers: chr4:g.74274495A>G (hg19) ; chr4:g.73408778A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408778A>G , CM000666.2:g.73408778A>G	GRCh38
NC_000004.11:g.74274495A>G , CM000666.1:g.74274495A>G	GRCh37
NC_000004.10:g.74493359A>G	NCBI36
NG_009291.1:g.9524A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.455A>G MANE Select	ENSP00000295897.4:p.His152Arg
ENST00000295897.8:c.455A>G	ENSP00000295897.4:p.His152Arg
ENST00000401494.7:c.138-577A>G	ENSP00000384695.3:n.138-577A>G
ENST00000415165.6:c.138-3218A>G	ENSP00000401820.2:n.138-3218A>G
ENST00000441319.5:c.461A>G	ENSP00000392541.1:p.His154Arg
ENST00000476441.6:c.80-577A>G	ENSP00000423727.1:n.80-577A>G
ENST00000503124.5:c.33-577A>G	ENSP00000421027.1:n.33-577A>G
ENST00000505649.5:n.141A>G
ENST00000509063.5:c.455A>G	ENSP00000422784.1:p.His152Arg
ENST00000510166.5:n.491A>G
ENST00000514786.1:n.424A>G
ENST00000515133.5:n.496A>G
ENST00000621085.4:c.455A>G	ENSP00000483421.1:p.His152Arg
ENST00000621628.4:c.455A>G	ENSP00000480485.1:p.His152Arg
NM_000477.5:c.455A>G	NP_000468.1:p.His152Arg
NM_000477.6:c.455A>G	NP_000468.1:p.His152Arg
NM_000477.7:c.455A>G MANE Select	NP_000468.1:p.His152Arg