Canonical Allele Identifier: CA2697570087
Gene:

Linked Data

dbSNP Id: rs1437636571
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121713A>G , CM000663.2:g.193121713A>G GRCh38
NC_000001.10:g.193090843A>G , CM000663.1:g.193090843A>G GRCh37
NC_000001.9:g.191357466A>G NCBI36
NG_012691.1:g.4756A>G , LRG_507:g.4756A>G

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1944T>C
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