Canonical Allele Identifier: CA2712751397
Gene:

Linked Data

dbSNP Id: rs2127980491
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102380C>T , CM000668.2:g.98102380C>T GRCh38
NC_000006.11:g.98550256C>T , CM000668.1:g.98550256C>T GRCh37
NC_000006.10:g.98656977C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.456+3110C>T
XR_942809.1:n.456+3110C>T
Search 100 bp 5'
Search 100 bp 3'