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Canonical Allele Identifier:
CA337771779
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.15458719C>T
GRCh37
chrY:g.17570599C>T
Linked Data - NCBI & NCI
dbSNP:
35516764
JSON-LD
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'