Canonical Allele Identifier: CA12308673
Gene:

Linked Data

dbSNP Id: rs12173570

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151636579C>T , CM000668.2:g.151636579C>T GRCh38
NC_000006.11:g.151957714C>T , CM000668.1:g.151957714C>T GRCh37
NC_000006.10:g.151999407C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943115.1:n.2496+6597C>T