Canonical Allele Identifier: CA2697150011
Gene: RNF115 HGNC NCBI

Linked Data

dbSNP Id: rs2101571580
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.145790099A>C , CM000663.2:g.145790099A>C GRCh38
NC_000001.10:g.145644982T>G , CM000663.1:g.145644982T>G GRCh37
NC_000001.9:g.144356339T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000582693.5:c.103-1133T>G MANE Select ENSP00000463650.1:n.103-1133T>G
ENST00000582693.4:c.103-1133T>G ENSP00000463650.1:n.103-1133T>G
NM_014455.3:c.103-1133T>G NP_055270.1:n.103-1133T>G
XM_005272952.3:c.-49-1133T>G XP_005273009.1:n.-49-1133T>G
XM_011509419.1:c.103-1133T>G XP_011507721.1:n.103-1133T>G
XM_005272952.5:c.-49-1133T>G XP_005273009.1:n.-49-1133T>G
XR_001737118.2:n.302-1133T>G
NM_014455.4:c.103-1133T>G MANE Select NP_055270.1:n.103-1133T>G
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