Canonical Allele Identifier: CA645372492
Gene:

Linked Data

MyVariant Identifiers: chr9:g.136500515T>T (hg19) chr9:g.133635393T>T (hg38)
PubMed: PMID:11170900 PMID:14991826 PMID:15505174 PMID:17503507 PMID:21509519
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133635393T= , CM000671.2:g.133635393T= GRCh38
NC_000009.11:g.136500515T= , CM000671.1:g.136500515T= GRCh37
NC_000009.10:g.135490336T= NCBI36
NG_008645.1:g.4031T=
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