Canonical Allele Identifier: CA2766266495
Gene: SRY HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2786964T>G , CM000686.2:g.2786964T>G GRCh38
NC_000024.9:g.2655005T>G , CM000686.1:g.2655005T>G GRCh37
NC_000024.8:g.2715005T>G NCBI36
NG_011751.1:g.5788A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+12225T>G
ENST00000679825.1:n.107-31T>G
ENST00000680285.1:n.320-2785T>G
ENST00000680845.1:n.107-31T>G
ENST00000681787.1:n.106+12225T>G
ENST00000681940.1:n.106+12225T>G
ENST00000383070.2:c.*25A>C MANE Select ENSP00000372547.1:n.*25A>C
ENST00000383070.1:c.*25A>C ENSP00000372547.1:n.*25A>C
NM_003140.2:c.*25A>C NP_003131.1:n.*25A>C
NM_003140.3:c.*25A>C MANE Select NP_003131.1:n.*25A>C
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