Canonical Allele Identifier: CA337437887
Gene: SRY HGNC NCBI

Linked Data

dbSNP Id: rs757482837
MyVariant Identifiers: chrY:g.2655008T>C (hg19) chrY:g.2786967T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2786967T>C , CM000686.2:g.2786967T>C GRCh38
NC_000024.9:g.2655008T>C , CM000686.1:g.2655008T>C GRCh37
NC_000024.8:g.2715008T>C NCBI36
NG_011751.1:g.5785A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12228T>C
ENST00000679825.1:n.107-28T>C
ENST00000680285.1:n.320-2782T>C
ENST00000680845.1:n.107-28T>C
ENST00000681787.1:n.106+12228T>C
ENST00000681940.1:n.106+12228T>C
ENST00000383070.2:c.*22A>G MANE Select ENSP00000372547.1:n.*22A>G
ENST00000383070.1:c.*22A>G ENSP00000372547.1:n.*22A>G
NM_003140.2:c.*22A>G NP_003131.1:n.*22A>G
NM_003140.3:c.*22A>G MANE Select NP_003131.1:n.*22A>G
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