Canonical Allele Identifier: CA357234383
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404334-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404334T>C , CM000666.2:g.73404334T>C GRCh38
NC_000004.11:g.74270051T>C , CM000666.1:g.74270051T>C GRCh37
NC_000004.10:g.74488915T>C NCBI36
NG_009291.1:g.5080T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.7T>C MANE Select ENSP00000295897.4:p.Trp3Arg
ENST00000295897.8:c.7T>C ENSP00000295897.4:p.Trp3Arg
ENST00000401494.7:c.7T>C ENSP00000384695.3:p.Trp3Arg
ENST00000415165.6:c.7T>C ENSP00000401820.2:p.Trp3Arg
ENST00000441319.5:c.48-35T>C ENSP00000392541.1:n.48-35T>C
ENST00000476441.6:c.7T>C ENSP00000423727.1:p.Trp3Arg
ENST00000503124.5:c.-174T>C ENSP00000421027.1:n.-174T>C
ENST00000509063.5:c.7T>C ENSP00000422784.1:p.Trp3Arg
ENST00000510166.5:n.48T>C
ENST00000514786.1:n.46T>C
ENST00000515133.5:n.48T>C
ENST00000621085.4:c.7T>C ENSP00000483421.1:p.Trp3Arg
ENST00000621628.4:c.7T>C ENSP00000480485.1:p.Trp3Arg
NM_000477.5:c.7T>C NP_000468.1:p.Trp3Arg
NM_000477.6:c.7T>C NP_000468.1:p.Trp3Arg
NM_000477.7:c.7T>C MANE Select NP_000468.1:p.Trp3Arg