Canonical Allele Identifier: CA2670936352
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404166G>T , CM000666.2:g.73404166G>T GRCh38
NC_000004.11:g.74269883G>T , CM000666.1:g.74269883G>T GRCh37
NC_000004.10:g.74488747G>T NCBI36
NG_009291.1:g.4912G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-203G>T ENSP00000392541.1:n.48-203G>T