Canonical Allele Identifier: CA357246605
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1281146594
gnomAD v3: 4-73419616-A-G
gnomAD v4: 4-73419616-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73419616A>G , CM000666.2:g.73419616A>G GRCh38
NC_000004.11:g.74285333A>G , CM000666.1:g.74285333A>G GRCh37
NC_000004.10:g.74504197A>G NCBI36
NG_009291.1:g.20362A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.1762A>G MANE Select ENSP00000295897.4:p.Lys588Glu
ENST00000295897.8:c.1762A>G ENSP00000295897.4:p.Lys588Glu
ENST00000401494.7:c.1417A>G ENSP00000384695.3:p.Lys473Glu
ENST00000415165.6:c.1186A>G ENSP00000401820.2:p.Lys396Glu
ENST00000476441.6:c.*1041A>G ENSP00000423727.1:n.*1041A>G
ENST00000495173.1:n.70A>G
ENST00000503124.5:c.1312A>G ENSP00000421027.1:p.Lys438Glu
ENST00000505649.5:n.1309A>G
ENST00000508932.5:n.175+161A>G
ENST00000509063.5:c.1762A>G ENSP00000422784.1:p.Lys588Glu
ENST00000511370.1:c.1295A>G
ENST00000621085.4:c.1123A>G ENSP00000483421.1:p.Lys375Glu
ENST00000621628.4:c.1123A>G ENSP00000480485.1:p.Lys375Glu
NM_000477.5:c.1762A>G NP_000468.1:p.Lys588Glu
NM_000477.6:c.1762A>G NP_000468.1:p.Lys588Glu
NM_000477.7:c.1762A>G MANE Select NP_000468.1:p.Lys588Glu