Canonical Allele Identifier: CA1947280471
Gene:

Linked Data

dbSNP Id: rs1339119125

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.747022C>T , CM000673.2:g.747022C>T GRCh38
NC_000011.9:g.747022C>T , CM000673.1:g.747022C>T GRCh37
NC_000011.8:g.737022C>T NCBI36
NG_008160.1:g.4591C>T

Transcript Alleles

HGVS Amino-acid change
XR_930963.1:n.259+173C>T