Canonical Allele Identifier: CA1468148647
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs748527302

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73420052C>A , CM000666.2:g.73420052C>A GRCh38
NC_000004.11:g.74285769C>A , CM000666.1:g.74285769C>A GRCh37
NC_000004.10:g.74504633C>A NCBI36
NG_009291.1:g.20798C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.1786-202C>A MANE Select ENSP00000295897.4:n.1786-202C>A
ENST00000295897.8:c.1786-202C>A ENSP00000295897.4:n.1786-202C>A
ENST00000401494.7:c.1441-202C>A ENSP00000384695.3:n.1441-202C>A
ENST00000415165.6:c.1210-202C>A ENSP00000401820.2:n.1210-202C>A
ENST00000476441.6:c.*1065-202C>A ENSP00000423727.1:n.*1065-202C>A
ENST00000495173.1:n.94-202C>A
ENST00000503124.5:c.1336-202C>A ENSP00000421027.1:n.1336-202C>A
ENST00000505649.5:n.1333-202C>A
ENST00000508932.5:n.176-202C>A
ENST00000509063.5:c.1785+413C>A ENSP00000422784.1:n.1785+413C>A
ENST00000511370.1:c.1319-202C>A
ENST00000621085.4:c.1147-202C>A ENSP00000483421.1:n.1147-202C>A
ENST00000621628.4:c.1147-202C>A ENSP00000480485.1:n.1147-202C>A
NM_000477.5:c.1786-202C>A NP_000468.1:n.1786-202C>A
NM_000477.6:c.1786-202C>A NP_000468.1:n.1786-202C>A
NM_000477.7:c.1786-202C>A MANE Select NP_000468.1:n.1786-202C>A