Canonical Allele Identifier: CA337771779
Gene:

Linked Data

dbSNP Id: rs35516764
MyVariant Identifiers: chrY:g.17570599C>T (hg19) chrY:g.15458719C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.15458719C>T , CM000686.2:g.15458719C>T GRCh38
NC_000024.9:g.17570599C>T , CM000686.1:g.17570599C>T GRCh37
NC_000024.8:g.16079993C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938614.1:n.81-1575C>T
Search 100 bp 5'
Search 100 bp 3'