Canonical Allele Identifier: CA390996210
Gene: RTL1 HGNC NCBI

Linked Data

dbSNP Id: rs1251441623
gnomAD v4: 14-100883363-T-C
MyVariant Identifiers: chr14:g.101349700T>C (hg19) chr14:g.100883363T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100883363T>C , CM000676.2:g.100883363T>C GRCh38
NC_000014.8:g.101349700T>C , CM000676.1:g.101349700T>C GRCh37
NC_000014.7:g.100419453T>C NCBI36
NG_045001.1:g.6485A>G
NG_045000.5:g.52095T>C
NG_045000.6:g.52095T>C
NG_045001.2:g.25360A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.1426A>G MANE Select ENSP00000497482.1:p.Thr476Ala
ENST00000534062.1:c.1426A>G ENSP00000435342.1:p.Thr476Ala
NM_001134888.2:c.1426A>G NP_001128360.1:p.Thr476Ala
NM_001134888.3:c.1426A>G MANE Select NP_001128360.1:p.Thr476Ala
Search 100 bp 5'
Search 100 bp 3'