ClinGen Allele Registry
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Canonical Allele Identifier:
CA136859085
Gene:
Linked Data
dbSNP Id:
rs6915220
gnomAD v2:
6-31407821-A-T
gnomAD v3:
6-31440044-A-T
gnomAD v4:
6-31440044-A-T
MyVariant Identifiers:
chr6:g.31407821A>T (hg19)
chr6:g.31440044A>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31440044A>T , CM000668.2:g.31440044A>T
GRCh38
NC_000006.11:g.31407821A>T , CM000668.1:g.31407821A>T
GRCh37
NC_000006.10:g.31515800A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_926694.1:n.63T>A
Search 100 bp 5'
Search 100 bp 3'