Canonical Allele Identifier: CA513685614
Gene:

Linked Data

MyVariant Identifiers: chr22:g.23915267G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573080G>C , CM000684.2:g.23573080G>C GRCh38
NC_000022.10:g.23915267G>C , CM000684.1:g.23915267G>C GRCh37
NC_000022.9:g.22245267G>C NCBI36
NG_009791.1:g.12229C>G , LRG_69:g.12229C>G

Transcript Alleles

HGVS Amino-acid Change
XR_938078.1:n.685G>C
XR_938078.2:n.1269G>C