Canonical Allele Identifier: CA513685589
Gene:

Linked Data

MyVariant Identifiers: chr22:g.23915259C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573072C>G , CM000684.2:g.23573072C>G GRCh38
NC_000022.10:g.23915259C>G , CM000684.1:g.23915259C>G GRCh37
NC_000022.9:g.22245259C>G NCBI36
NG_009791.1:g.12237G>C , LRG_69:g.12237G>C

Transcript Alleles

HGVS Amino-acid Change
XR_938075.1:n.713C>G
XR_938076.1:n.778C>G
XR_938078.1:n.677C>G
XR_938079.1:n.570C>G
XR_938075.2:n.1297C>G
XR_938078.2:n.1261C>G