Canonical Allele Identifier: CA861674172
Gene:

Linked Data

dbSNP Id: rs1419007933
MyVariant Identifiers: chr9:g.1787692A>C (hg19) chr9:g.1787692A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787692A>C , CM000671.2:g.1787692A>C GRCh38
NC_000009.11:g.1787692A>C , CM000671.1:g.1787692A>C GRCh37
NC_000009.10:g.1777692A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68780A>C
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