Canonical Allele Identifier: CA2698099663
Gene:

Linked Data

dbSNP Id: rs2102854282
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682373T>C , CM000663.2:g.213682373T>C GRCh38
NC_000001.10:g.213855716T>C , CM000663.1:g.213855716T>C GRCh37
NC_000001.9:g.211922339T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001738463.1:n.601-49044T>C
XR_001738464.1:n.426-49044T>C
Search 100 bp 5'
Search 100 bp 3'