Canonical Allele Identifier: CA660863583
Gene:

Linked Data

dbSNP Id: rs547330600
MyVariant Identifiers: chr10:g.124217605C>T (hg19) chr10:g.122458089C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122458089C>T , CM000672.2:g.122458089C>T GRCh38
NC_000010.10:g.124217605C>T , CM000672.1:g.124217605C>T GRCh37
NC_000010.9:g.124207595C>T NCBI36
NG_011554.1:g.1565C>T
NG_011725.1:g.8427C>T

Transcript Alleles

HGVS Amino-acid change
XR_946382.1:n.1827+406G>A
XR_946383.1:n.1827+406G>A
XR_946384.1:n.1576+406G>A
XR_946385.1:n.1827+406G>A
XR_946382.2:n.1855+406G>A
XR_946383.2:n.1855+406G>A
XR_946384.2:n.1580+406G>A
XR_946385.2:n.1855+406G>A
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