Canonical Allele Identifier: CA515479418
Gene: RS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.18690144G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18672024G>T , CM000685.2:g.18672024G>T GRCh38
NC_000023.10:g.18690144G>T , CM000685.1:g.18690144G>T GRCh37
NC_000023.9:g.18600065G>T NCBI36
NG_008659.3:g.10425C>A , LRG_702:g.10425C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379984.4:c.45C>A MANE Select ENSP00000369320.3:p.Gly15=
ENST00000379984.3:c.45C>A ENSP00000369320.3:p.Gly15=
NM_000330.3:c.45C>A , LRG_702t1:c.45C>A NP_000321.1:p.Gly15=
NM_000330.4:c.45C>A MANE Select NP_000321.1:p.Gly15=
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