Allele Registry

WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.

Canonical Allele Identifier: CA798282595

Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1216038759

MyVariant Identifiers: chr4:g.74269876T>C (hg19) chr4:g.73404159T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404159T>C , CM000666.2:g.73404159T>C	GRCh38
NC_000004.11:g.74269876T>C , CM000666.1:g.74269876T>C	GRCh37
NC_000004.10:g.74488740T>C	NCBI36
NG_009291.1:g.4905T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000441319.5:c.48-210T>C	ENSP00000392541.1:n.48-210T>C

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