Canonical Allele Identifier: CA414940978
Gene: SRY HGNC NCBI

Linked Data

dbSNP Id: rs2124485746

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787150C>T , CM000686.2:g.2787150C>T GRCh38
NC_000024.9:g.2655191C>T , CM000686.1:g.2655191C>T GRCh37
NC_000024.8:g.2715191C>T NCBI36
NG_011751.1:g.5602G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+12411C>T
ENST00000679825.1:n.262C>T
ENST00000680285.1:n.320-2599C>T
ENST00000680845.1:n.165+97C>T
ENST00000681787.1:n.106+12411C>T
ENST00000681940.1:n.106+12411C>T
ENST00000383070.2:c.454G>A MANE Select ENSP00000372547.1:p.Val152Ile
ENST00000383070.1:c.454G>A ENSP00000372547.1:p.Val152Ile
NM_003140.2:c.454G>A NP_003131.1:p.Val152Ile
NM_003140.3:c.454G>A MANE Select NP_003131.1:p.Val152Ile