Canonical Allele Identifier: CA1468148445
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404319T>G , CM000666.2:g.73404319T>G GRCh38
NC_000004.11:g.74270036T>G , CM000666.1:g.74270036T>G GRCh37
NC_000004.10:g.74488900T>G NCBI36
NG_009291.1:g.5065T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.-9T>G MANE Select ENSP00000295897.4:n.-9T>G
ENST00000295897.8:c.-9T>G ENSP00000295897.4:n.-9T>G
ENST00000401494.7:c.-9T>G ENSP00000384695.3:n.-9T>G
ENST00000415165.6:c.-9T>G ENSP00000401820.2:n.-9T>G
ENST00000441319.5:n.48-50T>G ENSP00000392541.1:n.48-50T>G
ENST00000476441.6:c.-9T>G ENSP00000423727.1:n.-9T>G
ENST00000503124.5:c.-189T>G ENSP00000421027.1:n.-189T>G
ENST00000509063.5:c.-9T>G ENSP00000422784.1:n.-9T>G
ENST00000510166.5:n.33T>G
ENST00000514786.1:n.31T>G
ENST00000515133.5:n.33T>G
ENST00000621085.4:c.-9T>G ENSP00000483421.1:n.-9T>G
ENST00000621628.4:c.-9T>G ENSP00000480485.1:n.-9T>G
NM_000477.5:c.-9T>G NP_000468.1:n.-9T>G
NM_000477.6:c.-9T>G NP_000468.1:n.-9T>G
NM_000477.7:c.-9T>G MANE Select NP_000468.1:n.-9T>G