Canonical Allele Identifier: CA422484977
Gene:

Linked Data

dbSNP Id: rs1286109709

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800720C>T , CM000663.2:g.192800720C>T GRCh38
NC_000001.10:g.192769850C>T , CM000663.1:g.192769850C>T GRCh37
NC_000001.9:g.191036473C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.150C>T