Canonical Allele Identifier: CA2697808973
Gene:

Linked Data

dbSNP Id: rs2103110636
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121752T>A , CM000663.2:g.193121752T>A GRCh38
NC_000001.10:g.193090882T>A , CM000663.1:g.193090882T>A GRCh37
NC_000001.9:g.191357505T>A NCBI36
NG_012691.1:g.4795T>A , LRG_507:g.4795T>A

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1905A>T
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