Canonical Allele Identifier: CA525878924
Gene: RNF115 HGNC NCBI

Linked Data

dbSNP Id: rs1553718748
gnomAD v2: 1-145644968-T-C
gnomAD v3: 1-145790113-A-G
gnomAD v4: 1-145790113-A-G
MyVariant Identifiers: chr1:g.145644968T>C (hg19) chr1:g.145790113A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.145790113A>G , CM000663.2:g.145790113A>G GRCh38
NC_000001.10:g.145644968T>C , CM000663.1:g.145644968T>C GRCh37
NC_000001.9:g.144356325T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000582693.5:c.103-1147T>C MANE Select ENSP00000463650.1:n.103-1147T>C
ENST00000582693.4:c.103-1147T>C ENSP00000463650.1:n.103-1147T>C
NM_014455.3:c.103-1147T>C NP_055270.1:n.103-1147T>C
XM_005272952.3:c.-49-1147T>C XP_005273009.1:n.-49-1147T>C
XM_011509419.1:c.103-1147T>C XP_011507721.1:n.103-1147T>C
XM_005272952.5:c.-49-1147T>C XP_005273009.1:n.-49-1147T>C
XR_001737118.2:n.302-1147T>C
NM_014455.4:c.103-1147T>C MANE Select NP_055270.1:n.103-1147T>C
Search 100 bp 5'
Search 100 bp 3'