Canonical Allele Identifier: CA64382937
Gene:

Linked Data

dbSNP Id: rs777648217
MyVariant Identifiers: chr2:g.200898033G>C (hg19) chr2:g.200033310G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033310G>C , CM000664.2:g.200033310G>C GRCh38
NC_000002.11:g.200898033G>C , CM000664.1:g.200898033G>C GRCh37
NC_000002.10:g.200606278G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22414C>G
Search 100 bp 5'
Search 100 bp 3'