Canonical Allele Identifier: CA1468148319

Gene: ALB

Linked Data

• dbSNP Id: rs1718657827
• gnomAD v4: 4-73404135-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404135T>C , CM000666.2:g.73404135T>C	GRCh38
NC_000004.11:g.74269852T>C , CM000666.1:g.74269852T>C	GRCh37
NC_000004.10:g.74488716T>C	NCBI36
NG_009291.1:g.4881T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000441319.5:c.48-234T>C	ENSP00000392541.1:n.48-234T>C