ClinGen Allele Registry
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Canonical Allele Identifier:
CA10701256
Gene: PROX1-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs17762192
gnomAD v2:
1-214125127-G-C
gnomAD v3:
1-213951784-G-C
gnomAD v4:
1-213951784-G-C
MyVariant Identifiers:
chr1:g.214125127G>C (hg19)
chr1:g.213951784G>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.213951784G>C , CM000663.2:g.213951784G>C
GRCh38
NC_000001.10:g.214125127G>C , CM000663.1:g.214125127G>C
GRCh37
NC_000001.9:g.212191750G>C
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_037850.2:n.299+14287C>G
Search 100 bp 5'
Search 100 bp 3'