Canonical Allele Identifier: CA107997239
Gene:

Linked Data

dbSNP Id: rs752636767

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748288C>T , CM000666.2:g.148748288C>T GRCh38
NC_000004.11:g.149669440C>T , CM000666.1:g.149669440C>T GRCh37
NC_000004.10:g.149888890C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741441.1:n.1746-118469C>T