Canonical Allele Identifier: CA2702620595
Gene:

Linked Data

dbSNP Id: rs2106643018

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428170C>T , CM000665.2:g.61428170C>T GRCh38
NC_000003.11:g.61413844C>T , CM000665.1:g.61413844C>T GRCh37
NC_000003.10:g.61388884C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940892.1:n.164+344G>A
XR_940893.1:n.164+344G>A
XR_001740725.1:n.202+344G>A
XR_940892.2:n.202+344G>A