Canonical Allele Identifier: CA1468143219
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1718973017

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73414829G>A , CM000666.2:g.73414829G>A GRCh38
NC_000004.11:g.74280546G>A , CM000666.1:g.74280546G>A GRCh37
NC_000004.10:g.74499410G>A NCBI36
NG_009291.1:g.15575G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.1059-206G>A MANE Select ENSP00000295897.4:n.1059-206G>A
ENST00000295897.8:c.1059-206G>A ENSP00000295897.4:n.1059-206G>A
ENST00000401494.7:c.714-206G>A ENSP00000384695.3:n.714-206G>A
ENST00000415165.6:c.483-206G>A ENSP00000401820.2:n.483-206G>A
ENST00000476441.6:c.*338-206G>A ENSP00000423727.1:n.*338-206G>A
ENST00000484992.1:n.379-206G>A
ENST00000503124.5:c.609-206G>A ENSP00000421027.1:n.609-206G>A
ENST00000504043.1:n.62-206G>A
ENST00000505649.5:n.745-206G>A
ENST00000509063.5:c.1059-206G>A ENSP00000422784.1:n.1059-206G>A
ENST00000511370.1:c.592-206G>A
ENST00000621085.4:c.491-277G>A ENSP00000483421.1:n.491-277G>A
ENST00000621628.4:c.487-273G>A ENSP00000480485.1:n.487-273G>A
NM_000477.5:c.1059-206G>A NP_000468.1:n.1059-206G>A
NM_000477.6:c.1059-206G>A NP_000468.1:n.1059-206G>A
NM_000477.7:c.1059-206G>A MANE Select NP_000468.1:n.1059-206G>A