Canonical Allele Identifier: CA357234349
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404331A>C , CM000666.2:g.73404331A>C GRCh38
NC_000004.11:g.74270048A>C , CM000666.1:g.74270048A>C GRCh37
NC_000004.10:g.74488912A>C NCBI36
NG_009291.1:g.5077A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.4A>C MANE Select ENSP00000295897.4:p.Lys2Gln
ENST00000295897.8:c.4A>C ENSP00000295897.4:p.Lys2Gln
ENST00000401494.7:c.4A>C ENSP00000384695.3:p.Lys2Gln
ENST00000415165.6:c.4A>C ENSP00000401820.2:p.Lys2Gln
ENST00000441319.5:n.48-38A>C ENSP00000392541.1:n.48-38A>C
ENST00000476441.6:c.4A>C ENSP00000423727.1:p.Lys2Gln
ENST00000503124.5:c.-177A>C ENSP00000421027.1:n.-177A>C
ENST00000509063.5:c.4A>C ENSP00000422784.1:p.Lys2Gln
ENST00000510166.5:n.45A>C
ENST00000514786.1:n.43A>C
ENST00000515133.5:n.45A>C
ENST00000621085.4:c.4A>C ENSP00000483421.1:p.Lys2Gln
ENST00000621628.4:c.4A>C ENSP00000480485.1:p.Lys2Gln
NM_000477.5:c.4A>C NP_000468.1:p.Lys2Gln
NM_000477.6:c.4A>C NP_000468.1:p.Lys2Gln
NM_000477.7:c.4A>C MANE Select NP_000468.1:p.Lys2Gln