Canonical Allele Identifier: CA1573962529
Gene:

Linked Data

dbSNP Id: rs1780760442
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113714823C>T , CM000667.2:g.113714823C>T GRCh38
NC_000005.9:g.113050520C>T , CM000667.1:g.113050520C>T GRCh37
NC_000005.8:g.113078419C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742840.1:n.153-18738C>T
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Search 100 bp 3'