Canonical Allele Identifier: CA422484980
Gene:

Linked Data

dbSNP Id: rs1235100431

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800721C>G , CM000663.2:g.192800721C>G GRCh38
NC_000001.10:g.192769851C>G , CM000663.1:g.192769851C>G GRCh37
NC_000001.9:g.191036474C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.151C>G