Canonical Allele Identifier: CA798282528
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1217641336
MyVariant Identifiers: chr4:g.74269782del (hg19) chr4:g.73404065del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404065del , CM000666.2:g.73404065del GRCh38
NC_000004.11:g.74269782del , CM000666.1:g.74269782del GRCh37
NC_000004.10:g.74488646del NCBI36
NG_009291.1:g.4811del

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-304del ENSP00000392541.1:n.48-304del
Search 100 bp 5'
Search 100 bp 3'