Canonical Allele Identifier: CA464226005
Gene:

Linked Data

dbSNP Id: rs1181916168
gnomAD v3: 9-25551364-G-A
gnomAD v4: 9-25551364-G-A
MyVariant Identifiers: chr9:g.25551362G>A (hg19) chr9:g.25551364G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551364G>A , CM000671.2:g.25551364G>A GRCh38
NC_000009.11:g.25551362G>A , CM000671.1:g.25551362G>A GRCh37
NC_000009.10:g.25541362G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-792C>T
XR_929525.2:n.674-792C>T
Search 100 bp 5'
Search 100 bp 3'