Canonical Allele Identifier: CA1468148392
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404284G= , CM000666.2:g.73404284G= GRCh38
NC_000004.11:g.74270001G= , CM000666.1:g.74270001G= GRCh37
NC_000004.10:g.74488865G= NCBI36
NG_009291.1:g.5030G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.8:c.-44G= ENSP00000295897.4:n.-44G=
ENST00000441319.5:c.48-85G= ENSP00000392541.1:n.48-85G=
ENST00000621628.4:c.-44G= ENSP00000480485.1:n.-44G=
NM_000477.5:c.-44G= NP_000468.1:n.-44G=
NM_000477.6:c.-44G= NP_000468.1:n.-44G=