Canonical Allele Identifier: CA735235341
Gene:

Linked Data

dbSNP Id: rs1197214362
MyVariant Identifiers: chr1:g.34989213C>T (hg19) chr1:g.34523612C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523612C>T , CM000663.2:g.34523612C>T GRCh38
NC_000001.10:g.34989213C>T , CM000663.1:g.34989213C>T GRCh37
NC_000001.9:g.34761800C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947171.1:n.1073+23967G>A
XR_001737964.1:n.991+23967G>A
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