Canonical Allele Identifier: CA357238271

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275166T>C (hg19) ; chr4:g.73409449T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409449T>C , CM000666.2:g.73409449T>C	GRCh38
NC_000004.11:g.74275166T>C , CM000666.1:g.74275166T>C	GRCh37
NC_000004.10:g.74494030T>C	NCBI36
NG_009291.1:g.10195T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.577T>C MANE Select	ENSP00000295897.4:p.Cys193Arg
ENST00000295897.8:c.577T>C	ENSP00000295897.4:p.Cys193Arg
ENST00000401494.7:c.232T>C	ENSP00000384695.3:p.Cys78Arg
ENST00000415165.6:c.138-2547T>C	ENSP00000401820.2:n.138-2547T>C
ENST00000441319.5:c.583T>C	ENSP00000392541.1:p.Cys195Arg
ENST00000476441.6:c.174T>C	ENSP00000423727.1:p.Val58=
ENST00000503124.5:c.127T>C	ENSP00000421027.1:p.Cys43Arg
ENST00000505649.5:n.263T>C
ENST00000509063.5:c.577T>C	ENSP00000422784.1:p.Cys193Arg
ENST00000511370.1:c.110T>C
ENST00000514786.1:n.546T>C
ENST00000621085.4:c.490+87T>C	ENSP00000483421.1:n.490+87T>C
ENST00000621628.4:c.486+373T>C	ENSP00000480485.1:n.486+373T>C
NM_000477.5:c.577T>C	NP_000468.1:p.Cys193Arg
NM_000477.6:c.577T>C	NP_000468.1:p.Cys193Arg
NM_000477.7:c.577T>C MANE Select	NP_000468.1:p.Cys193Arg