Canonical Allele Identifier: CA188145873
Gene:

Linked Data

dbSNP Id: rs959819604
MyVariant Identifiers: chr9:g.1787613T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787613T>G , CM000671.2:g.1787613T>G GRCh38
NC_000009.11:g.1787613T>G , CM000671.1:g.1787613T>G GRCh37
NC_000009.10:g.1777613T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746599.1:n.142+68701T>G