Canonical Allele Identifier: CA266904675
Gene: RTL1 HGNC NCBI

Linked Data

dbSNP Id: rs755600518
gnomAD v2: 14-101349035-C-T
gnomAD v3: 14-100882698-C-T
gnomAD v4: 14-100882698-C-T
MyVariant Identifiers: chr14:g.101349035C>T (hg19) chr14:g.100882698C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100882698C>T , CM000676.2:g.100882698C>T GRCh38
NC_000014.8:g.101349035C>T , CM000676.1:g.101349035C>T GRCh37
NC_000014.7:g.100418788C>T NCBI36
NG_045001.1:g.7150G>A
NG_045000.5:g.51430C>T
NG_045000.6:g.51430C>T
NG_045001.2:g.26025G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.2091G>A MANE Select ENSP00000497482.1:p.Met697Ile
ENST00000534062.1:c.2091G>A ENSP00000435342.1:p.Met697Ile
NM_001134888.2:c.2091G>A NP_001128360.1:p.Met697Ile
NM_001134888.3:c.2091G>A MANE Select NP_001128360.1:p.Met697Ile
Search 100 bp 5'
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