Canonical Allele Identifier: CA414940703
Gene: SRY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2655074A>C (hg19) chrY:g.2787033A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787033A>C , CM000686.2:g.2787033A>C GRCh38
NC_000024.9:g.2655074A>C , CM000686.1:g.2655074A>C GRCh37
NC_000024.8:g.2715074A>C NCBI36
NG_011751.1:g.5719T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12294A>C
ENST00000679825.1:n.145A>C
ENST00000680285.1:n.320-2716A>C
ENST00000680845.1:n.145A>C
ENST00000681787.1:n.106+12294A>C
ENST00000681940.1:n.106+12294A>C
ENST00000383070.2:c.571T>G MANE Select ENSP00000372547.1:p.Ser191Ala
ENST00000383070.1:c.571T>G ENSP00000372547.1:p.Ser191Ala
NM_003140.2:c.571T>G NP_003131.1:p.Ser191Ala
NM_003140.3:c.571T>G MANE Select NP_003131.1:p.Ser191Ala
Search 100 bp 5'
Search 100 bp 3'