Canonical Allele Identifier: CA414941933
Gene: SRY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2655601T>G (hg19) chrY:g.2787560T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787560T>G , CM000686.2:g.2787560T>G GRCh38
NC_000024.9:g.2655601T>G , CM000686.1:g.2655601T>G GRCh37
NC_000024.8:g.2715601T>G NCBI36
NG_011751.1:g.5192A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12821T>G
ENST00000679825.1:n.672T>G
ENST00000680285.1:n.320-2189T>G
ENST00000680845.1:n.246T>G
ENST00000681787.1:n.106+12821T>G
ENST00000681940.1:n.106+12821T>G
ENST00000383070.2:c.44A>C MANE Select ENSP00000372547.1:p.Asp15Ala
ENST00000383070.1:c.44A>C ENSP00000372547.1:p.Asp15Ala
NM_003140.2:c.44A>C NP_003131.1:p.Asp15Ala
NM_003140.3:c.44A>C MANE Select NP_003131.1:p.Asp15Ala
Search 100 bp 5'
Search 100 bp 3'