Canonical Allele Identifier: CA214412891
Gene:

Linked Data

dbSNP Id: rs774134745
MyVariant Identifiers: chr10:g.124217654T>G (hg19) chr10:g.122458138T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122458138T>G , CM000672.2:g.122458138T>G GRCh38
NC_000010.10:g.124217654T>G , CM000672.1:g.124217654T>G GRCh37
NC_000010.9:g.124207644T>G NCBI36
NG_011554.1:g.1614T>G
NG_011725.1:g.8476T>G

Transcript Alleles

HGVS Amino-acid change
XR_946382.1:n.1827+357A>C
XR_946383.1:n.1827+357A>C
XR_946384.1:n.1576+357A>C
XR_946385.1:n.1827+357A>C
XR_946382.2:n.1855+357A>C
XR_946383.2:n.1855+357A>C
XR_946384.2:n.1580+357A>C
XR_946385.2:n.1855+357A>C
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