Canonical Allele Identifier: CA1216113087
Gene:

Linked Data

dbSNP Id: rs1675446108
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121722T>C , CM000663.2:g.193121722T>C GRCh38
NC_000001.10:g.193090852T>C , CM000663.1:g.193090852T>C GRCh37
NC_000001.9:g.191357475T>C NCBI36
NG_012691.1:g.4765T>C , LRG_507:g.4765T>C

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1935A>G
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