Canonical Allele Identifier: CA2959540
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 349625
ClinVar RCV Id: RCV000379657
dbSNP Id: rs370277014
gnomAD v2: 4-74280741-A-G
gnomAD v3: 4-73415024-A-G
gnomAD v4: 4-73415024-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73415024A>G , CM000666.2:g.73415024A>G GRCh38
NC_000004.11:g.74280741A>G , CM000666.1:g.74280741A>G GRCh37
NC_000004.10:g.74499605A>G NCBI36
NG_009291.1:g.15770A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1059-11A>G MANE Select ENSP00000295897.4:n.1059-11A>G
ENST00000295897.8:c.1059-11A>G ENSP00000295897.4:n.1059-11A>G
ENST00000401494.7:c.714-11A>G ENSP00000384695.3:n.714-11A>G
ENST00000415165.6:c.483-11A>G ENSP00000401820.2:n.483-11A>G
ENST00000476441.6:c.*338-11A>G ENSP00000423727.1:n.*338-11A>G
ENST00000484992.1:n.379-11A>G
ENST00000503124.5:c.609-11A>G ENSP00000421027.1:n.609-11A>G
ENST00000504043.1:n.62-11A>G
ENST00000505649.5:n.745-11A>G
ENST00000509063.5:c.1059-11A>G ENSP00000422784.1:n.1059-11A>G
ENST00000511370.1:c.592-11A>G
ENST00000621085.4:c.491-82A>G ENSP00000483421.1:n.491-82A>G
ENST00000621628.4:c.487-78A>G ENSP00000480485.1:n.487-78A>G
NM_000477.5:c.1059-11A>G NP_000468.1:n.1059-11A>G
NM_000477.6:c.1059-11A>G NP_000468.1:n.1059-11A>G
NM_000477.7:c.1059-11A>G MANE Select NP_000468.1:n.1059-11A>G