Canonical Allele Identifier: CA99696945

Gene: ALB

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73405117C>A , CM000666.2:g.73405117C>A	GRCh38
NC_000004.11:g.74270834C>A , CM000666.1:g.74270834C>A	GRCh37
NC_000004.10:g.74489698C>A	NCBI36
NG_009291.1:g.5863C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.81C>A MANE Select	ENSP00000295897.4:p.His27Gln
ENST00000295897.8:c.81C>A	ENSP00000295897.4:p.His27Gln
ENST00000401494.7:c.81C>A	ENSP00000384695.3:p.His27Gln
ENST00000415165.6:c.81C>A	ENSP00000401820.2:p.His27Gln
ENST00000441319.5:c.87C>A	ENSP00000392541.1:p.His29Gln
ENST00000476441.6:c.79+711C>A	ENSP00000423727.1:n.79+711C>A
ENST00000503124.5:c.-102+711C>A	ENSP00000421027.1:n.-102+711C>A
ENST00000509063.5:c.81C>A	ENSP00000422784.1:p.His27Gln
ENST00000510166.5:n.121-4C>A
ENST00000514786.1:n.50C>A
ENST00000515133.5:n.122C>A
ENST00000621085.4:c.81C>A	ENSP00000483421.1:p.His27Gln
ENST00000621628.4:c.81C>A	ENSP00000480485.1:p.His27Gln
NM_000477.5:c.81C>A	NP_000468.1:p.His27Gln
NM_000477.6:c.81C>A	NP_000468.1:p.His27Gln
NM_000477.7:c.81C>A MANE Select	NP_000468.1:p.His27Gln