Canonical Allele Identifier: CA488181947
Gene: RTL1 HGNC NCBI

Linked Data

dbSNP Id: rs1450278450
gnomAD v2: 14-101349890-C-T
gnomAD v4: 14-100883553-C-T
MyVariant Identifiers: chr14:g.101349890C>T (hg19) chr14:g.100883553C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100883553C>T , CM000676.2:g.100883553C>T GRCh38
NC_000014.8:g.101349890C>T , CM000676.1:g.101349890C>T GRCh37
NC_000014.7:g.100419643C>T NCBI36
NG_045001.1:g.6295G>A
NG_045000.5:g.52285C>T
NG_045000.6:g.52285C>T
NG_045001.2:g.25170G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.1236G>A MANE Select ENSP00000497482.1:p.Leu412=
ENST00000534062.1:c.1236G>A ENSP00000435342.1:p.Leu412=
NM_001134888.2:c.1236G>A NP_001128360.1:p.Leu412=
NM_001134888.3:c.1236G>A MANE Select NP_001128360.1:p.Leu412=
Search 100 bp 5'
Search 100 bp 3'