Canonical Allele Identifier: CA211665910
Gene:

Linked Data

dbSNP Id: rs997814902
MyVariant Identifiers: chr10:g.94762418C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762418C>T , CM000672.2:g.94762418C>T GRCh38
NC_000010.10:g.96522175C>T , CM000672.1:g.96522175C>T GRCh37
NC_000010.9:g.96512165C>T NCBI36
NG_008384.2:g.4713C>T
NG_008384.3:g.4738C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12640C>T ENSP00000483243.1:n.932-12640C>T
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