Canonical Allele Identifier: CA337593993
Gene: RFTN1P1 HGNC NCBI

Linked Data

dbSNP Id: rs181270813
gnomAD v4: Y-7736269-G-T
MyVariant Identifiers: chrY:g.7604310G>T (hg19) chrY:g.7736269G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7736269G>T , CM000686.2:g.7736269G>T GRCh38
NC_000024.9:g.7604310G>T , CM000686.1:g.7604310G>T GRCh37
NC_000024.8:g.7664310G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651261.1:n.299-23172C>A
ENST00000455527.5:n.297-6429C>A
Search 100 bp 5'
Search 100 bp 3'