Canonical Allele Identifier: CA798282616

Gene: ALB

Linked Data

• dbSNP Id: rs1429489541
• MyVariant Identifiers: chr4:g.74269936del (hg19) ; chr4:g.73404219del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404219del , CM000666.2:g.73404219del	GRCh38
NC_000004.11:g.74269936del , CM000666.1:g.74269936del	GRCh37
NC_000004.10:g.74488800del	NCBI36
NG_009291.1:g.4965del

Transcript Alleles

HGVS	Amino-acid change
ENST00000441319.5:c.48-150del	ENSP00000392541.1:n.48-150del