Canonical Allele Identifier: CA660863561
Gene:

Linked Data

dbSNP Id: rs1392816095
MyVariant Identifiers: chr10:g.124217471C>T (hg19) chr10:g.122457955C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122457955C>T , CM000672.2:g.122457955C>T GRCh38
NC_000010.10:g.124217471C>T , CM000672.1:g.124217471C>T GRCh37
NC_000010.9:g.124207461C>T NCBI36
NG_011554.1:g.1431C>T
NG_011725.1:g.8293C>T

Transcript Alleles

HGVS Amino-acid Change
XR_946382.1:n.1827+540G>A
XR_946383.1:n.1827+540G>A
XR_946384.1:n.1576+540G>A
XR_946385.1:n.1827+540G>A
XR_946382.2:n.1855+540G>A
XR_946383.2:n.1855+540G>A
XR_946384.2:n.1580+540G>A
XR_946385.2:n.1855+540G>A
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