Canonical Allele Identifier: CA151622551
Gene:

Linked Data

dbSNP Id: rs937935474

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765673C>T , CM000668.2:g.163765673C>T GRCh38
NC_000006.11:g.164186705C>T , CM000668.1:g.164186705C>T GRCh37
NC_000006.10:g.164106695C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6244C>T
XR_001744454.1:n.369+6285C>T
XR_001744455.1:n.346+6308C>T