Canonical Allele Identifier: CA414941949
Gene: SRY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2655607T>G (hg19) chrY:g.2787566T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787566T>G , CM000686.2:g.2787566T>G GRCh38
NC_000024.9:g.2655607T>G , CM000686.1:g.2655607T>G GRCh37
NC_000024.8:g.2715607T>G NCBI36
NG_011751.1:g.5186A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12827T>G
ENST00000679825.1:n.678T>G
ENST00000680285.1:n.320-2183T>G
ENST00000680845.1:n.252T>G
ENST00000681787.1:n.106+12827T>G
ENST00000681940.1:n.106+12827T>G
ENST00000383070.2:c.38A>C MANE Select ENSP00000372547.1:p.Asn13Thr
ENST00000383070.1:c.38A>C ENSP00000372547.1:p.Asn13Thr
NM_003140.2:c.38A>C NP_003131.1:p.Asn13Thr
NM_003140.3:c.38A>C MANE Select NP_003131.1:p.Asn13Thr
Search 100 bp 5'
Search 100 bp 3'