Canonical Allele Identifier: CA414940648
Gene: SRY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2655049C>G (hg19) chrY:g.2787008C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787008C>G , CM000686.2:g.2787008C>G GRCh38
NC_000024.9:g.2655049C>G , CM000686.1:g.2655049C>G GRCh37
NC_000024.8:g.2715049C>G NCBI36
NG_011751.1:g.5744G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12269C>G
ENST00000679825.1:n.120C>G
ENST00000680285.1:n.320-2741C>G
ENST00000680845.1:n.120C>G
ENST00000681787.1:n.106+12269C>G
ENST00000681940.1:n.106+12269C>G
ENST00000383070.2:c.596G>C MANE Select ENSP00000372547.1:p.Ser199Thr
ENST00000383070.1:c.596G>C ENSP00000372547.1:p.Ser199Thr
NM_003140.2:c.596G>C NP_003131.1:p.Ser199Thr
NM_003140.3:c.596G>C MANE Select NP_003131.1:p.Ser199Thr
Search 100 bp 5'
Search 100 bp 3'