Canonical Allele Identifier: CA519724323
Gene: SRY HGNC NCBI

Linked Data

dbSNP Id: rs2124485943
MyVariant Identifiers: chrY:g.2655279C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787238C>T , CM000686.2:g.2787238C>T GRCh38
NC_000024.9:g.2655279C>T , CM000686.1:g.2655279C>T GRCh37
NC_000024.8:g.2715279C>T NCBI36
NG_011751.1:g.5514G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+12499C>T
ENST00000679825.1:n.350C>T
ENST00000680285.1:n.320-2511C>T
ENST00000680845.1:n.165+185C>T
ENST00000681787.1:n.106+12499C>T
ENST00000681940.1:n.106+12499C>T
ENST00000383070.2:c.366G>A MANE Select ENSP00000372547.1:p.Glu122=
ENST00000383070.1:c.366G>A ENSP00000372547.1:p.Glu122=
NM_003140.2:c.366G>A NP_003131.1:p.Glu122=
NM_003140.3:c.366G>A MANE Select NP_003131.1:p.Glu122=