Canonical Allele Identifier: CA60480231
Gene:

Linked Data

dbSNP Id: rs998597520
MyVariant Identifiers: chr2:g.169116993C>T (hg19) chr2:g.168260483C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168260483C>T , CM000664.2:g.168260483C>T GRCh38
NC_000002.11:g.169116993C>T , CM000664.1:g.169116993C>T GRCh37
NC_000002.10:g.168825239C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739763.1:n.912-4613C>T
XR_001739764.1:n.318-4613C>T
XR_001739765.1:n.436-4613C>T
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