Canonical Allele Identifier: CA2573054147

Gene:

Linked Data

• ClinVar Variation Id: 1330139
• ClinVar RCV Id: RCV001801156
• dbSNP Id: rs1555449252

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.172834C>T , CM000678.2:g.172834C>T	GRCh38
NC_000016.9:g.222833C>T , CM000678.1:g.222833C>T	GRCh37
NC_000016.8:g.162833C>T	NCBI36
NG_000006.1:g.33697C>T
NG_059186.1:g.1184C>T
NG_059271.1:g.4988C>T