Canonical Allele Identifier: CA13273915
Gene:

Linked Data

dbSNP Id: rs10883688
gnomAD v2: 10-103510393-A-C
gnomAD v3: 10-101750636-A-C
gnomAD v4: 10-101750636-A-C
MyVariant Identifiers: chr10:g.103510393A>C (hg19) chr10:g.101750636A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101750636A>C , CM000672.2:g.101750636A>C GRCh38
NC_000010.10:g.103510393A>C , CM000672.1:g.103510393A>C GRCh37
NC_000010.9:g.103500383A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946255.1:n.217-6419T>G
XR_946255.2:n.217-6419T>G
Search 100 bp 5'
Search 100 bp 3'