Canonical Allele Identifier: CA414941112
Gene: SRY HGNC NCBI

Linked Data

dbSNP Id: rs2124485891

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787210G>C , CM000686.2:g.2787210G>C GRCh38
NC_000024.9:g.2655251G>C , CM000686.1:g.2655251G>C GRCh37
NC_000024.8:g.2715251G>C NCBI36
NG_011751.1:g.5542C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+12471G>C
ENST00000679825.1:n.322G>C
ENST00000680285.1:n.320-2539G>C
ENST00000680845.1:n.165+157G>C
ENST00000681787.1:n.106+12471G>C
ENST00000681940.1:n.106+12471G>C
ENST00000383070.2:c.394C>G MANE Select ENSP00000372547.1:p.Arg132Gly
ENST00000383070.1:c.394C>G ENSP00000372547.1:p.Arg132Gly
NM_003140.2:c.394C>G NP_003131.1:p.Arg132Gly
NM_003140.3:c.394C>G MANE Select NP_003131.1:p.Arg132Gly