Canonical Allele Identifier: CA1320446215
Gene:

Linked Data

dbSNP Id: rs2077889500
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033305G>C , CM000664.2:g.200033305G>C GRCh38
NC_000002.11:g.200898028G>C , CM000664.1:g.200898028G>C GRCh37
NC_000002.10:g.200606273G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22409C>G
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Search 100 bp 3'