Canonical Allele Identifier: CA276765519

Gene: NTHL1

Linked Data

• dbSNP Id: rs574467357
• gnomAD v3: 16-2046054-A-C
• gnomAD v4: 16-2046054-A-C
• MyVariant Identifiers: chr16:g.2096055A>C (hg19) ; chr16:g.2046054A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046054A>C , CM000678.2:g.2046054A>C	GRCh38
NC_000016.9:g.2096055A>C , CM000678.1:g.2096055A>C	GRCh37
NC_000016.8:g.2036056A>C	NCBI36
NG_005895.1:g.1749A>C , LRG_487:g.1749A>C
NG_008412.1:g.6813T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000651522.1:c.63+74T>G	ENSP00000498290.1:n.63+74T>G
ENST00000651570.2:c.354+74T>G MANE Select	ENSP00000498421.1:n.354+74T>G
ENST00000651583.1:c.309+74T>G	ENSP00000498821.1:n.309+74T>G
ENST00000219066.5:c.378+74T>G	ENSP00000219066.1:n.378+74T>G
ENST00000561841.1:c.274+74T>G
ENST00000562120.1:n.87+74T>G
ENST00000566380.5:c.317+74T>G
ENST00000568513.5:c.173+226T>G
NM_002528.5:c.378+74T>G	NP_002519.1:n.378+74T>G
XM_011522505.1:c.378+74T>G	XP_011520807.1:n.378+74T>G
NM_001318193.1:c.378+74T>G	NP_001305122.1:n.378+74T>G
NM_001318194.1:c.24+226T>G	NP_001305123.1:n.24+226T>G
NM_002528.6:c.378+74T>G	NP_002519.1:n.378+74T>G
XM_017023253.1:c.378+74T>G	XP_016878742.1:n.378+74T>G
NM_001318193.2:c.354+74T>G	NP_001305122.2:n.354+74T>G
NM_002528.7:c.354+74T>G MANE Select	NP_002519.2:n.354+74T>G
NM_001318194.2:c.24+226T>G	NP_001305123.1:n.24+226T>G