Canonical Allele Identifier: CA2417997019
Gene: RS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18672063T= , CM000685.2:g.18672063T= GRCh38
NC_000023.10:g.18690183T= , CM000685.1:g.18690183T= GRCh37
NC_000023.9:g.18600104T= NCBI36
NG_008659.3:g.10386A= , LRG_702:g.10386A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379984.4:c.6A= MANE Select ENSP00000369320.3:p.Ser2=
ENST00000379984.3:c.6A= ENSP00000369320.3:p.Ser2=
NM_000330.3:c.6A= , LRG_702t1:c.6A= NP_000321.1:p.Ser2=
NM_000330.4:c.6A= MANE Select NP_000321.1:p.Ser2=
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