Canonical Allele Identifier: CA1468148283
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1718655772

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404071T>C , CM000666.2:g.73404071T>C GRCh38
NC_000004.11:g.74269788T>C , CM000666.1:g.74269788T>C GRCh37
NC_000004.10:g.74488652T>C NCBI36
NG_009291.1:g.4817T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-298T>C ENSP00000392541.1:n.48-298T>C