Canonical Allele Identifier: CA2697808990
Gene:

Linked Data

dbSNP Id: rs2103110672
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121773T>G , CM000663.2:g.193121773T>G GRCh38
NC_000001.10:g.193090903T>G , CM000663.1:g.193090903T>G GRCh37
NC_000001.9:g.191357526T>G NCBI36
NG_012691.1:g.4816T>G , LRG_507:g.4816T>G

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1884A>C
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