Canonical Allele Identifier: CA2122202171
Gene:

Linked Data

dbSNP Id: rs1879066558

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20793447C>T , CM000676.2:g.20793447C>T GRCh38
NC_000014.8:g.21261606C>T , CM000676.1:g.21261606C>T GRCh37
NC_000014.7:g.20331446C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943584.1:n.585+661C>T
XR_943585.1:n.585+661C>T
XR_001750620.1:n.3271+661C>T
XR_001750621.1:n.3271+661C>T
XR_001750622.1:n.637+6457G>A
XR_001750623.1:n.637+6457G>A
XR_001750624.1:n.637+6457G>A