Canonical Allele Identifier: CA2697809079
Gene:

Linked Data

dbSNP Id: rs2103110705
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121784C>T , CM000663.2:g.193121784C>T GRCh38
NC_000001.10:g.193090914C>T , CM000663.1:g.193090914C>T GRCh37
NC_000001.9:g.191357537C>T NCBI36
NG_012691.1:g.4827C>T , LRG_507:g.4827C>T

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1873G>A
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