Canonical Allele Identifier: CA519724013
Gene: SRY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2655129T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787088T>C , CM000686.2:g.2787088T>C GRCh38
NC_000024.9:g.2655129T>C , CM000686.1:g.2655129T>C GRCh37
NC_000024.8:g.2715129T>C NCBI36
NG_011751.1:g.5664A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+12349T>C
ENST00000679825.1:n.200T>C
ENST00000680285.1:n.320-2661T>C
ENST00000680845.1:n.165+35T>C
ENST00000681787.1:n.106+12349T>C
ENST00000681940.1:n.106+12349T>C
ENST00000383070.2:c.516A>G MANE Select ENSP00000372547.1:p.Thr172=
ENST00000383070.1:c.516A>G ENSP00000372547.1:p.Thr172=
NM_003140.2:c.516A>G NP_003131.1:p.Thr172=
NM_003140.3:c.516A>G MANE Select NP_003131.1:p.Thr172=
Search 100 bp 5'
Search 100 bp 3'