Canonical Allele Identifier: CA1010607996
Gene:

Linked Data

dbSNP Id: rs1675451773

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121886A>G , CM000663.2:g.193121886A>G GRCh38
NC_000001.10:g.193091016A>G , CM000663.1:g.193091016A>G GRCh37
NC_000001.9:g.191357639A>G NCBI36
NG_012691.1:g.4929A>G , LRG_507:g.4929A>G

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1771T>C