Canonical Allele Identifier: CA337704786
Gene: ASS1P6 HGNC NCBI

Linked Data

dbSNP Id: rs112327544
MyVariant Identifiers: chrY:g.14043535C>A (hg19) chrY:g.11922829C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.11922829C>A , CM000686.2:g.11922829C>A GRCh38
NC_000024.9:g.14043535C>A , CM000686.1:g.14043535C>A GRCh37
NC_000024.8:g.12553535C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000421118.1:n.941G>T
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