Canonical Allele Identifier: CA390996338
Gene: RTL1 HGNC NCBI

Linked Data

dbSNP Id: rs2140036585
gnomAD v4: 14-100883424-G-T
MyVariant Identifiers: chr14:g.101349761G>T (hg19) chr14:g.100883424G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100883424G>T , CM000676.2:g.100883424G>T GRCh38
NC_000014.8:g.101349761G>T , CM000676.1:g.101349761G>T GRCh37
NC_000014.7:g.100419514G>T NCBI36
NG_045001.1:g.6424C>A
NG_045000.5:g.52156G>T
NG_045000.6:g.52156G>T
NG_045001.2:g.25299C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.1365C>A MANE Select ENSP00000497482.1:p.Tyr455Ter
ENST00000534062.1:c.1365C>A ENSP00000435342.1:p.Tyr455Ter
NM_001134888.2:c.1365C>A NP_001128360.1:p.Tyr455Ter
NM_001134888.3:c.1365C>A MANE Select NP_001128360.1:p.Tyr455Ter
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