Canonical Allele Identifier: CA1468148379
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1718660584

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404278C>T , CM000666.2:g.73404278C>T GRCh38
NC_000004.11:g.74269995C>T , CM000666.1:g.74269995C>T GRCh37
NC_000004.10:g.74488859C>T NCBI36
NG_009291.1:g.5024C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-50C>T ENSP00000295897.4:n.-50C>T
ENST00000441319.5:c.48-91C>T ENSP00000392541.1:n.48-91C>T
ENST00000621628.4:c.-50C>T ENSP00000480485.1:n.-50C>T
NM_000477.5:c.-50C>T NP_000468.1:n.-50C>T
NM_000477.6:c.-50C>T NP_000468.1:n.-50C>T