Canonical Allele Identifier: CA357241075

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280765T>C (hg19) ; chr4:g.73415048T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415048T>C , CM000666.2:g.73415048T>C	GRCh38
NC_000004.11:g.74280765T>C , CM000666.1:g.74280765T>C	GRCh37
NC_000004.10:g.74499629T>C	NCBI36
NG_009291.1:g.15794T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1072T>C MANE Select	ENSP00000295897.4:p.Tyr358His
ENST00000295897.8:c.1072T>C	ENSP00000295897.4:p.Tyr358His
ENST00000401494.7:c.727T>C	ENSP00000384695.3:p.Tyr243His
ENST00000415165.6:c.496T>C	ENSP00000401820.2:p.Tyr166His
ENST00000476441.6:c.*351T>C	ENSP00000423727.1:n.*351T>C
ENST00000484992.1:n.392T>C
ENST00000503124.5:c.622T>C	ENSP00000421027.1:p.Tyr208His
ENST00000504043.1:n.75T>C
ENST00000505649.5:n.758T>C
ENST00000509063.5:c.1072T>C	ENSP00000422784.1:p.Tyr358His
ENST00000511370.1:c.605T>C
ENST00000621085.4:c.491-58T>C	ENSP00000483421.1:n.491-58T>C
ENST00000621628.4:c.487-54T>C	ENSP00000480485.1:n.487-54T>C
NM_000477.5:c.1072T>C	NP_000468.1:p.Tyr358His
NM_000477.6:c.1072T>C	NP_000468.1:p.Tyr358His
NM_000477.7:c.1072T>C MANE Select	NP_000468.1:p.Tyr358His