Canonical Allele Identifier: CA439800265
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1222187655
gnomAD v2: 4-74280774-A-C
gnomAD v3: 4-73415057-A-C
gnomAD v4: 4-73415057-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73415057A>C , CM000666.2:g.73415057A>C GRCh38
NC_000004.11:g.74280774A>C , CM000666.1:g.74280774A>C GRCh37
NC_000004.10:g.74499638A>C NCBI36
NG_009291.1:g.15803A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1081A>C MANE Select ENSP00000295897.4:p.Arg361=
ENST00000295897.8:c.1081A>C ENSP00000295897.4:p.Arg361=
ENST00000401494.7:c.736A>C ENSP00000384695.3:p.Arg246=
ENST00000415165.6:c.505A>C ENSP00000401820.2:p.Arg169=
ENST00000476441.6:c.*360A>C ENSP00000423727.1:n.*360A>C
ENST00000484992.1:n.401A>C
ENST00000503124.5:c.631A>C ENSP00000421027.1:p.Arg211=
ENST00000504043.1:n.84A>C
ENST00000505649.5:n.767A>C
ENST00000509063.5:c.1081A>C ENSP00000422784.1:p.Arg361=
ENST00000511370.1:c.614A>C
ENST00000621085.4:c.491-49A>C ENSP00000483421.1:n.491-49A>C
ENST00000621628.4:c.487-45A>C ENSP00000480485.1:n.487-45A>C
NM_000477.5:c.1081A>C NP_000468.1:p.Arg361=
NM_000477.6:c.1081A>C NP_000468.1:p.Arg361=
NM_000477.7:c.1081A>C MANE Select NP_000468.1:p.Arg361=