Canonical Allele Identifier: CA357241118
Gene: ALB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73415060C>T , CM000666.2:g.73415060C>T GRCh38
NC_000004.11:g.74280777C>T , CM000666.1:g.74280777C>T GRCh37
NC_000004.10:g.74499641C>T NCBI36
NG_009291.1:g.15806C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1084C>T MANE Select ENSP00000295897.4:p.His362Tyr
ENST00000295897.8:c.1084C>T ENSP00000295897.4:p.His362Tyr
ENST00000401494.7:c.739C>T ENSP00000384695.3:p.His247Tyr
ENST00000415165.6:c.508C>T ENSP00000401820.2:p.His170Tyr
ENST00000476441.6:c.*363C>T ENSP00000423727.1:n.*363C>T
ENST00000484992.1:n.404C>T
ENST00000503124.5:c.634C>T ENSP00000421027.1:p.His212Tyr
ENST00000504043.1:n.87C>T
ENST00000505649.5:n.770C>T
ENST00000509063.5:c.1084C>T ENSP00000422784.1:p.His362Tyr
ENST00000511370.1:c.617C>T
ENST00000621085.4:c.491-46C>T ENSP00000483421.1:n.491-46C>T
ENST00000621628.4:c.487-42C>T ENSP00000480485.1:n.487-42C>T
NM_000477.5:c.1084C>T NP_000468.1:p.His362Tyr
NM_000477.6:c.1084C>T NP_000468.1:p.His362Tyr
NM_000477.7:c.1084C>T MANE Select NP_000468.1:p.His362Tyr