Canonical Allele Identifier: CA414941370
Gene: SRY HGNC NCBI

Linked Data

ClinVar Variation Id: 537738
ClinVar RCV Id: RCV000646759
dbSNP Id: rs1556370548
MyVariant Identifiers: chrY:g.2655357G>C (hg19) chrY:g.2787316G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787316G>C , CM000686.2:g.2787316G>C GRCh38
NC_000024.9:g.2655357G>C , CM000686.1:g.2655357G>C GRCh37
NC_000024.8:g.2715357G>C NCBI36
NG_011751.1:g.5436C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+12577G>C
ENST00000679825.1:n.428G>C
ENST00000680285.1:n.320-2433G>C
ENST00000680845.1:n.166-164G>C
ENST00000681787.1:n.106+12577G>C
ENST00000681940.1:n.106+12577G>C
ENST00000383070.2:c.288C>G MANE Select ENSP00000372547.1:p.Tyr96Ter
ENST00000383070.1:c.288C>G ENSP00000372547.1:p.Tyr96Ter
NM_003140.2:c.288C>G NP_003131.1:p.Tyr96Ter
NM_003140.3:c.288C>G MANE Select NP_003131.1:p.Tyr96Ter
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