Canonical Allele Identifier: CA1678638513
Gene:

Linked Data

dbSNP Id: rs1780708468

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765694T>C , CM000668.2:g.163765694T>C GRCh38
NC_000006.11:g.164186726T>C , CM000668.1:g.164186726T>C GRCh37
NC_000006.10:g.164106716T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6265T>C
XR_001744454.1:n.369+6306T>C
XR_001744455.1:n.346+6329T>C