Canonical Allele Identifier: CA492953193
Gene: NTHL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.2096141A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2046140A>G , CM000678.2:g.2046140A>G GRCh38
NC_000016.9:g.2096141A>G , CM000678.1:g.2096141A>G GRCh37
NC_000016.8:g.2036142A>G NCBI36
NG_005895.1:g.1835A>G , LRG_487:g.1835A>G
NG_008412.1:g.6727T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651522.1:c.51T>C ENSP00000498290.1:p.Ser17=
ENST00000651570.2:c.342T>C MANE Select ENSP00000498421.1:p.Ser114=
ENST00000651583.1:c.297T>C ENSP00000498821.1:p.Ser99=
ENST00000219066.5:c.366T>C ENSP00000219066.1:p.Ser122=
ENST00000561841.1:c.262T>C
ENST00000562120.1:n.75T>C
ENST00000566380.5:c.305T>C
ENST00000568513.5:c.173+140T>C
NM_002528.5:c.366T>C NP_002519.1:p.Ser122=
XM_011522505.1:c.366T>C XP_011520807.1:p.Ser122=
NM_001318193.1:c.366T>C NP_001305122.1:p.Ser122=
NM_001318194.1:c.24+140T>C NP_001305123.1:n.24+140T>C
NM_002528.6:c.366T>C NP_002519.1:p.Ser122=
XM_017023253.1:c.366T>C XP_016878742.1:p.Ser122=
NM_001318193.2:c.342T>C NP_001305122.2:p.Ser114=
NM_002528.7:c.342T>C MANE Select NP_002519.2:p.Ser114=
NM_001318194.2:c.24+140T>C NP_001305123.1:n.24+140T>C