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Canonical Allele Identifier:
CA337705259
Gene: MXRA5Y
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.11958822T>C
GRCh37
chrY:g.14079528T>C
Linked Data - NCBI & NCI
dbSNP:
113195977
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.11958822T>C , CM000686.2:g.11958822T>C
GRCh38
NC_000024.9:g.14079528T>C , CM000686.1:g.14079528T>C
GRCh37
NC_000024.8:g.12589528T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000420610.1:n.192+1423T>C
Search 100 bp 5'
Search 100 bp 3'