Canonical Allele Identifier: CA337593778
Gene: RFTN1P1 HGNC NCBI

Linked Data

dbSNP Id: rs909122412
MyVariant Identifiers: chrY:g.7587023C>T (hg19) chrY:g.7718982C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7718982C>T , CM000686.2:g.7718982C>T GRCh38
NC_000024.9:g.7587023C>T , CM000686.1:g.7587023C>T GRCh37
NC_000024.8:g.7647023C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651261.1:n.299-5885G>A
ENST00000455527.5:n.883+2874G>A
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