Canonical Allele Identifier: CA357241123

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280779T>G (hg19) ; chr4:g.73415062T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415062T>G , CM000666.2:g.73415062T>G	GRCh38
NC_000004.11:g.74280779T>G , CM000666.1:g.74280779T>G	GRCh37
NC_000004.10:g.74499643T>G	NCBI36
NG_009291.1:g.15808T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1086T>G MANE Select	ENSP00000295897.4:p.His362Gln
ENST00000295897.8:c.1086T>G	ENSP00000295897.4:p.His362Gln
ENST00000401494.7:c.741T>G	ENSP00000384695.3:p.His247Gln
ENST00000415165.6:c.510T>G	ENSP00000401820.2:p.His170Gln
ENST00000476441.6:c.*365T>G	ENSP00000423727.1:n.*365T>G
ENST00000484992.1:n.406T>G
ENST00000503124.5:c.636T>G	ENSP00000421027.1:p.His212Gln
ENST00000504043.1:n.89T>G
ENST00000505649.5:n.772T>G
ENST00000509063.5:c.1086T>G	ENSP00000422784.1:p.His362Gln
ENST00000511370.1:c.619T>G
ENST00000621085.4:c.491-44T>G	ENSP00000483421.1:n.491-44T>G
ENST00000621628.4:c.487-40T>G	ENSP00000480485.1:n.487-40T>G
NM_000477.5:c.1086T>G	NP_000468.1:p.His362Gln
NM_000477.6:c.1086T>G	NP_000468.1:p.His362Gln
NM_000477.7:c.1086T>G MANE Select	NP_000468.1:p.His362Gln