Canonical Allele Identifier: CA357236405

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74274326G>C (hg19) ; chr4:g.73408609G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408609G>C , CM000666.2:g.73408609G>C	GRCh38
NC_000004.11:g.74274326G>C , CM000666.1:g.74274326G>C	GRCh37
NC_000004.10:g.74493190G>C	NCBI36
NG_009291.1:g.9355G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.286G>C MANE Select	ENSP00000295897.4:p.Asp96His
ENST00000295897.8:c.286G>C	ENSP00000295897.4:p.Asp96His
ENST00000401494.7:c.138-746G>C	ENSP00000384695.3:n.138-746G>C
ENST00000415165.6:c.138-3387G>C	ENSP00000401820.2:n.138-3387G>C
ENST00000441319.5:c.292G>C	ENSP00000392541.1:p.Asp98His
ENST00000476441.6:c.80-746G>C	ENSP00000423727.1:n.80-746G>C
ENST00000503124.5:c.33-746G>C	ENSP00000421027.1:n.33-746G>C
ENST00000509063.5:c.286G>C	ENSP00000422784.1:p.Asp96His
ENST00000510166.5:n.322G>C
ENST00000514786.1:n.255G>C
ENST00000515133.5:n.327G>C
ENST00000621085.4:c.286G>C	ENSP00000483421.1:p.Asp96His
ENST00000621628.4:c.286G>C	ENSP00000480485.1:p.Asp96His
NM_000477.5:c.286G>C	NP_000468.1:p.Asp96His
NM_000477.6:c.286G>C	NP_000468.1:p.Asp96His
NM_000477.7:c.286G>C MANE Select	NP_000468.1:p.Asp96His