Canonical Allele Identifier: CA46769626
Gene:

Linked Data

dbSNP Id: rs753449182
MyVariant Identifiers: chr2:g.41761876C>G (hg19) chr2:g.41534736C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534736C>G , CM000664.2:g.41534736C>G GRCh38
NC_000002.11:g.41761876C>G , CM000664.1:g.41761876C>G GRCh37
NC_000002.10:g.41615380C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939996.1:n.181+2990G>C
XR_939997.1:n.146+2990G>C
XR_939997.2:n.9529+2990G>C
Search 100 bp 5'
Search 100 bp 3'