Canonical Allele Identifier: CA488181462
Gene: RTL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.101349113G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.100882776G>C , CM000676.2:g.100882776G>C GRCh38
NC_000014.8:g.101349113G>C , CM000676.1:g.101349113G>C GRCh37
NC_000014.7:g.100418866G>C NCBI36
NG_045001.1:g.7072C>G
NG_045000.5:g.51508G>C
NG_045000.6:g.51508G>C
NG_045001.2:g.25947C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000649591.1:c.2013C>G MANE Select ENSP00000497482.1:p.Thr671=
ENST00000534062.1:c.2013C>G ENSP00000435342.1:p.Thr671=
NM_001134888.2:c.2013C>G NP_001128360.1:p.Thr671=
NM_001134888.3:c.2013C>G MANE Select NP_001128360.1:p.Thr671=
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