Canonical Allele Identifier: CA170820

Gene: ALB

Linked Data

• ClinVar Variation Id: 156315
• ClinVar RCV Id: RCV000144399
• dbSNP Id: rs79738788
• MyVariant Identifiers: chr4:g.74285292A>C (hg19) ; chr4:g.73419575A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419575A>C , CM000666.2:g.73419575A>C	GRCh38
NC_000004.11:g.74285292A>C , CM000666.1:g.74285292A>C	GRCh37
NC_000004.10:g.74504156A>C	NCBI36
NG_009291.1:g.20321A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1721A>C MANE Select	ENSP00000295897.4:p.Asp574Ala
ENST00000295897.8:c.1721A>C	ENSP00000295897.4:p.Asp574Ala
ENST00000401494.7:c.1376A>C	ENSP00000384695.3:p.Asp459Ala
ENST00000415165.6:c.1145A>C	ENSP00000401820.2:p.Asp382Ala
ENST00000476441.6:c.*1000A>C	ENSP00000423727.1:n.*1000A>C
ENST00000495173.1:n.29A>C
ENST00000503124.5:c.1271A>C	ENSP00000421027.1:p.Asp424Ala
ENST00000505649.5:n.1268A>C
ENST00000508932.5:n.175+120A>C
ENST00000509063.5:c.1721A>C	ENSP00000422784.1:p.Asp574Ala
ENST00000511370.1:c.1254A>C
ENST00000621085.4:c.1082A>C	ENSP00000483421.1:p.Asp361Ala
ENST00000621628.4:c.1082A>C	ENSP00000480485.1:p.Asp361Ala
NM_000477.5:c.1721A>C	NP_000468.1:p.Asp574Ala
NM_000477.6:c.1721A>C	NP_000468.1:p.Asp574Ala
NM_000477.7:c.1721A>C MANE Select	NP_000468.1:p.Asp574Ala