Canonical Allele Identifier: CA2542164197
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404312A>T , CM000666.2:g.73404312A>T GRCh38
NC_000004.11:g.74270029A>T , CM000666.1:g.74270029A>T GRCh37
NC_000004.10:g.74488893A>T NCBI36
NG_009291.1:g.5058A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.-16A>T MANE Select ENSP00000295897.4:n.-16A>T
ENST00000295897.8:c.-16A>T ENSP00000295897.4:n.-16A>T
ENST00000401494.7:c.-16A>T ENSP00000384695.3:n.-16A>T
ENST00000415165.6:c.-16A>T ENSP00000401820.2:n.-16A>T
ENST00000441319.5:n.48-57A>T ENSP00000392541.1:n.48-57A>T
ENST00000476441.6:c.-16A>T ENSP00000423727.1:n.-16A>T
ENST00000503124.5:c.-196A>T ENSP00000421027.1:n.-196A>T
ENST00000509063.5:c.-16A>T ENSP00000422784.1:n.-16A>T
ENST00000510166.5:n.26A>T
ENST00000514786.1:n.24A>T
ENST00000515133.5:n.26A>T
ENST00000621085.4:c.-16A>T ENSP00000483421.1:n.-16A>T
ENST00000621628.4:c.-16A>T ENSP00000480485.1:n.-16A>T
NM_000477.5:c.-16A>T NP_000468.1:n.-16A>T
NM_000477.6:c.-16A>T NP_000468.1:n.-16A>T
NM_000477.7:c.-16A>T MANE Select NP_000468.1:n.-16A>T