Canonical Allele Identifier: CA2697809573
Gene:

Linked Data

dbSNP Id: rs2103110923
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121892G>A , CM000663.2:g.193121892G>A GRCh38
NC_000001.10:g.193091022G>A , CM000663.1:g.193091022G>A GRCh37
NC_000001.9:g.191357645G>A NCBI36
NG_012691.1:g.4935G>A , LRG_507:g.4935G>A

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1765C>T
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