Canonical Allele Identifier: CA357240545

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74279177T>C (hg19) ; chr4:g.73413460T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413460T>C , CM000666.2:g.73413460T>C	GRCh38
NC_000004.11:g.74279177T>C , CM000666.1:g.74279177T>C	GRCh37
NC_000004.10:g.74498041T>C	NCBI36
NG_009291.1:g.14206T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.884T>C MANE Select	ENSP00000295897.4:p.Ile295Thr
ENST00000295897.8:c.884T>C	ENSP00000295897.4:p.Ile295Thr
ENST00000401494.7:c.539T>C	ENSP00000384695.3:p.Ile180Thr
ENST00000415165.6:c.308T>C	ENSP00000401820.2:p.Ile103Thr
ENST00000476441.6:c.*163T>C	ENSP00000423727.1:n.*163T>C
ENST00000484992.1:n.204T>C
ENST00000503124.5:c.434T>C	ENSP00000421027.1:p.Ile145Thr
ENST00000505649.5:n.570T>C
ENST00000509063.5:c.884T>C	ENSP00000422784.1:p.Ile295Thr
ENST00000511370.1:c.417T>C
ENST00000621085.4:c.491-1646T>C	ENSP00000483421.1:n.491-1646T>C
ENST00000621628.4:c.487-1642T>C	ENSP00000480485.1:n.487-1642T>C
NM_000477.5:c.884T>C	NP_000468.1:p.Ile295Thr
NM_000477.6:c.884T>C	NP_000468.1:p.Ile295Thr
NM_000477.7:c.884T>C MANE Select	NP_000468.1:p.Ile295Thr