Canonical Allele Identifier: CA2698684811
Gene:

Linked Data

dbSNP Id: rs2103349997
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458310T>C , CM000664.2:g.16458310T>C GRCh38
NC_000002.11:g.16639578T>C , CM000664.1:g.16639578T>C GRCh37
NC_000002.10:g.16503059T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939752.1:n.396-3216A>G
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