Canonical Allele Identifier: CA2606574619
Gene:

Linked Data

dbSNP Id: rs2103110654

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121759C>G , CM000663.2:g.193121759C>G GRCh38
NC_000001.10:g.193090889C>G , CM000663.1:g.193090889C>G GRCh37
NC_000001.9:g.191357512C>G NCBI36
NG_012691.1:g.4802C>G , LRG_507:g.4802C>G

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1898G>C