Canonical Allele Identifier: CA880383585
Gene: RFTN1P1 HGNC NCBI

Linked Data

dbSNP Id: rs1250535203
MyVariant Identifiers: chrY:g.7645376G>C (hg19) chrY:g.7777335G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7777335G>C , CM000686.2:g.7777335G>C GRCh38
NC_000024.9:g.7645376G>C , CM000686.1:g.7645376G>C GRCh37
NC_000024.8:g.7705376G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651261.1:n.115-631C>G
ENST00000652723.1:n.1027-631C>G
ENST00000442584.2:n.219-307C>G
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