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Canonical Allele Identifier:
CA337645120
Gene: RBMY2QP
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.9973185C>T
GRCh37
chrY:g.9810794C>T
Linked Data - Sequence & Population
gnomAD v3:
Y:9973185 C / T
gnomAD v4:
chrY-9973185-C-T
Joint Max Group AF
0.978091 (AFR)
Genomes Max Group AF
0.978091 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7067387
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.9973185C>T , CM000686.2:g.9973185C>T
GRCh38
NC_000024.9:g.9810794C>T , CM000686.1:g.9810794C>T
GRCh37
NC_000024.8:g.10420794C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000651645.1:n.1003+16005G>A
Search 100 bp 5'
Search 100 bp 3'