Canonical Allele Identifier: CA1345190
Gene: KISS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1274010
ClinVar RCV Id: RCV001684998
dbSNP Id: rs35431622
ExAC: 1:204159922 T / C
gnomAD v2: 1-204159922-T-C
gnomAD v3: 1-204190794-T-C
gnomAD v4: 1-204190794-T-C
MyVariant Identifiers: chr1:g.204159922T>C (hg19) chr1:g.204190794T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204190794T>C , CM000663.2:g.204190794T>C GRCh38
NC_000001.10:g.204159922T>C , CM000663.1:g.204159922T>C GRCh37
NC_000001.9:g.202426545T>C NCBI36
NG_032151.1:g.10698A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367194.5:c.107A>G MANE Select ENSP00000356162.4:p.Gln36Arg
ENST00000367194.4:c.107A>G ENSP00000356162.4:p.Gln36Arg
ENST00000625357.1:c.107A>G ENSP00000485957.1:p.Gln36Arg
NM_002256.3:c.107A>G NP_002247.3:p.Gln36Arg
XM_011509525.1:c.107A>G XP_011507827.1:p.Gln36Arg
NM_002256.4:c.107A>G MANE Select NP_002247.3:p.Gln36Arg
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