Canonical Allele Identifier: CA2959253
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs764560163
gnomAD v2: 4-74270102-G-C
gnomAD v4: 4-73404385-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404385G>C , CM000666.2:g.73404385G>C GRCh38
NC_000004.11:g.74270102G>C , CM000666.1:g.74270102G>C GRCh37
NC_000004.10:g.74488966G>C NCBI36
NG_009291.1:g.5131G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.58G>C MANE Select ENSP00000295897.4:p.Gly20Arg
ENST00000295897.8:c.58G>C ENSP00000295897.4:p.Gly20Arg
ENST00000401494.7:c.58G>C ENSP00000384695.3:p.Gly20Arg
ENST00000415165.6:c.58G>C ENSP00000401820.2:p.Gly20Arg
ENST00000441319.5:c.64G>C ENSP00000392541.1:p.Gly22Arg
ENST00000476441.6:c.58G>C ENSP00000423727.1:p.Gly20Arg
ENST00000503124.5:c.-123G>C ENSP00000421027.1:n.-123G>C
ENST00000509063.5:c.58G>C ENSP00000422784.1:p.Gly20Arg
ENST00000510166.5:n.99G>C
ENST00000514786.1:n.48+49G>C
ENST00000515133.5:n.99G>C
ENST00000621085.4:c.58G>C ENSP00000483421.1:p.Gly20Arg
ENST00000621628.4:c.58G>C ENSP00000480485.1:p.Gly20Arg
NM_000477.5:c.58G>C NP_000468.1:p.Gly20Arg
NM_000477.6:c.58G>C NP_000468.1:p.Gly20Arg
NM_000477.7:c.58G>C MANE Select NP_000468.1:p.Gly20Arg