Canonical Allele Identifier: CA99696375
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs893689870

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404317C>G , CM000666.2:g.73404317C>G GRCh38
NC_000004.11:g.74270034C>G , CM000666.1:g.74270034C>G GRCh37
NC_000004.10:g.74488898C>G NCBI36
NG_009291.1:g.5063C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.-11C>G MANE Select ENSP00000295897.4:n.-11C>G
ENST00000295897.8:c.-11C>G ENSP00000295897.4:n.-11C>G
ENST00000401494.7:c.-11C>G ENSP00000384695.3:n.-11C>G
ENST00000415165.6:c.-11C>G ENSP00000401820.2:n.-11C>G
ENST00000441319.5:n.48-52C>G ENSP00000392541.1:n.48-52C>G
ENST00000476441.6:c.-11C>G ENSP00000423727.1:n.-11C>G
ENST00000503124.5:c.-191C>G ENSP00000421027.1:n.-191C>G
ENST00000509063.5:c.-11C>G ENSP00000422784.1:n.-11C>G
ENST00000510166.5:n.31C>G
ENST00000514786.1:n.29C>G
ENST00000515133.5:n.31C>G
ENST00000621085.4:c.-11C>G ENSP00000483421.1:n.-11C>G
ENST00000621628.4:c.-11C>G ENSP00000480485.1:n.-11C>G
NM_000477.5:c.-11C>G NP_000468.1:n.-11C>G
NM_000477.6:c.-11C>G NP_000468.1:n.-11C>G
NM_000477.7:c.-11C>G MANE Select NP_000468.1:n.-11C>G