Canonical Allele Identifier: CA2417996978
Gene: RS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18671934A= , CM000685.2:g.18671934A= GRCh38
NC_000023.10:g.18690054A= , CM000685.1:g.18690054A= GRCh37
NC_000023.9:g.18599975A= NCBI36
NG_008659.3:g.10515T= , LRG_702:g.10515T=

Transcript Alleles

HGVS Amino-acid change
ENST00000379984.4:c.52+83T= MANE Select ENSP00000369320.3:n.52+83T=
ENST00000379984.3:c.52+83T= ENSP00000369320.3:n.52+83T=
NM_000330.3:c.52+83T= , LRG_702t1:c.52+83T= NP_000321.1:n.52+83T=
NM_000330.4:c.52+83T= MANE Select NP_000321.1:n.52+83T=