Canonical Allele Identifier: CA1678638491
Gene:

Linked Data

dbSNP Id: rs1562624593

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765650T>C , CM000668.2:g.163765650T>C GRCh38
NC_000006.11:g.164186682T>C , CM000668.1:g.164186682T>C GRCh37
NC_000006.10:g.164106672T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6221T>C
XR_001744454.1:n.369+6262T>C
XR_001744455.1:n.346+6285T>C