Canonical Allele Identifier: CA2579746170
Gene: SRY HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2786928G>T , CM000686.2:g.2786928G>T GRCh38
NC_000024.9:g.2654969G>T , CM000686.1:g.2654969G>T GRCh37
NC_000024.8:g.2714969G>T NCBI36
NG_011751.1:g.5824C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+12189G>T
ENST00000679825.1:n.107-67G>T
ENST00000680285.1:n.320-2821G>T
ENST00000680845.1:n.107-67G>T
ENST00000681787.1:n.106+12189G>T
ENST00000681940.1:n.106+12189G>T
ENST00000383070.2:c.*61C>A MANE Select ENSP00000372547.1:n.*61C>A
ENST00000383070.1:c.*61C>A ENSP00000372547.1:n.*61C>A
NM_003140.2:c.*61C>A NP_003131.1:n.*61C>A
NM_003140.3:c.*61C>A MANE Select NP_003131.1:n.*61C>A
Search 100 bp 5'
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