Canonical Allele Identifier: CA337350305
Gene: TTTY14 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.19063884C>G
GRCh37 chrY:g.21225770C>G
gnomAD v3:
Y:19063884 C / G
gnomAD v4:
chrY-19063884-C-G
Joint Max Group AF 0.26403608 (MID)
Genomes Max Group AF 0.22928008 (NFE)
dbSNP:
17250163
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19063884C>G , CM000686.2:g.19063884C>G GRCh38
NC_000024.9:g.21225770C>G , CM000686.1:g.21225770C>G GRCh37
NC_000024.8:g.19685158C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_001543.3:n.560-5284G>C
NR_125733.1:n.578+4840G>C
NR_125734.1:n.578+4840G>C
NR_125735.1:n.503+13161G>C
NR_125736.1:n.138+4840G>C
NR_125737.1:n.138+4840G>C
NR_001543.4:n.503+13161G>C
NR_125737.2:n.138+4840G>C
NR_158640.1:n.152+9615G>C
NR_158641.1:n.164+4840G>C
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