Canonical Allele Identifier: CA2698684823
Gene:

Linked Data

dbSNP Id: rs2103350019
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458392T>C , CM000664.2:g.16458392T>C GRCh38
NC_000002.11:g.16639660T>C , CM000664.1:g.16639660T>C GRCh37
NC_000002.10:g.16503141T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939752.1:n.396-3298A>G
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Search 100 bp 3'