Canonical Allele Identifier: CA717349455
Gene:

Linked Data

dbSNP Id: rs925783079
MyVariant Identifiers: chr15:g.95318536C>G (hg19) chr15:g.94775307C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.94775307C>G , CM000677.2:g.94775307C>G GRCh38
NC_000015.9:g.95318536C>G , CM000677.1:g.95318536C>G GRCh37
NC_000015.8:g.93119540C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932644.1:n.369-9290G>C
XR_932644.2:n.369-9290G>C
Search 100 bp 5'
Search 100 bp 3'