Canonical Allele Identifier: CA764797567
Gene: DIRC3 HGNC NCBI

Linked Data

dbSNP Id: rs6759952
MyVariant Identifiers: chr2:g.218271719T>A (hg19) chr2:g.217406996T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.217406996T>A , CM000664.2:g.217406996T>A GRCh38
NC_000002.11:g.218271719T>A , CM000664.1:g.218271719T>A GRCh37
NC_000002.10:g.217979964T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474063.5:n.1458+18306A>T
ENST00000486365.5:n.2290+18306A>T
NR_026597.1:n.2290+18306A>T
NR_026597.2:n.2290+18306A>T
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