Canonical Allele Identifier: CA660863696
Gene:

Linked Data

dbSNP Id: rs1255704370
MyVariant Identifiers: chr10:g.124217797C>A (hg19) chr10:g.122458281C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122458281C>A , CM000672.2:g.122458281C>A GRCh38
NC_000010.10:g.124217797C>A , CM000672.1:g.124217797C>A GRCh37
NC_000010.9:g.124207787C>A NCBI36
NG_011554.1:g.1757C>A
NG_011725.1:g.8619C>A

Transcript Alleles

HGVS Amino-acid Change
XR_946382.1:n.1827+214G>T
XR_946383.1:n.1827+214G>T
XR_946384.1:n.1576+214G>T
XR_946385.1:n.1827+214G>T
XR_946382.2:n.1855+214G>T
XR_946383.2:n.1855+214G>T
XR_946384.2:n.1580+214G>T
XR_946385.2:n.1855+214G>T
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