Canonical Allele Identifier: CA552304300
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1328463373
gnomAD v2: 4-74270335-C-T
gnomAD v3: 4-73404618-C-T
gnomAD v4: 4-73404618-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404618C>T , CM000666.2:g.73404618C>T GRCh38
NC_000004.11:g.74270335C>T , CM000666.1:g.74270335C>T GRCh37
NC_000004.10:g.74489199C>T NCBI36
NG_009291.1:g.5364C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.79+212C>T MANE Select ENSP00000295897.4:n.79+212C>T
ENST00000295897.8:c.79+212C>T ENSP00000295897.4:n.79+212C>T
ENST00000401494.7:c.79+212C>T ENSP00000384695.3:n.79+212C>T
ENST00000415165.6:c.79+212C>T ENSP00000401820.2:n.79+212C>T
ENST00000441319.5:c.85+212C>T ENSP00000392541.1:n.85+212C>T
ENST00000476441.6:c.79+212C>T ENSP00000423727.1:n.79+212C>T
ENST00000503124.5:c.-102+212C>T ENSP00000421027.1:n.-102+212C>T
ENST00000509063.5:c.79+212C>T ENSP00000422784.1:n.79+212C>T
ENST00000510166.5:n.120+212C>T
ENST00000514786.1:n.48+282C>T
ENST00000515133.5:n.120+212C>T
ENST00000621085.4:c.79+212C>T ENSP00000483421.1:n.79+212C>T
ENST00000621628.4:c.79+212C>T ENSP00000480485.1:n.79+212C>T
NM_000477.5:c.79+212C>T NP_000468.1:n.79+212C>T
NM_000477.6:c.79+212C>T NP_000468.1:n.79+212C>T
NM_000477.7:c.79+212C>T MANE Select NP_000468.1:n.79+212C>T