Canonical Allele Identifier: CA394297122

Gene: NTHL1

Linked Data

• dbSNP Id: rs2150946078
• MyVariant Identifiers: chr16:g.2096230G>A (hg19) ; chr16:g.2046229G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046229G>A , CM000678.2:g.2046229G>A	GRCh38
NC_000016.9:g.2096230G>A , CM000678.1:g.2096230G>A	GRCh37
NC_000016.8:g.2036231G>A	NCBI36
NG_005895.1:g.1924G>A , LRG_487:g.1924G>A
NG_008412.1:g.6638C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651570.2:c.253C>T MANE Select	ENSP00000498421.1:p.Gln85Ter
ENST00000651583.1:c.208C>T	ENSP00000498821.1:p.Gln70Ter
ENST00000219066.5:c.277C>T	ENSP00000219066.1:p.Gln93Ter
ENST00000561841.1:c.173C>T
ENST00000566380.5:c.216C>T
ENST00000568513.5:c.173+51C>T
NM_002528.5:c.277C>T	NP_002519.1:p.Gln93Ter
XM_011522505.1:c.277C>T	XP_011520807.1:p.Gln93Ter
NM_001318193.1:c.277C>T	NP_001305122.1:p.Gln93Ter
NM_001318194.1:c.24+51C>T	NP_001305123.1:n.24+51C>T
NM_002528.6:c.277C>T	NP_002519.1:p.Gln93Ter
XM_017023253.1:c.277C>T	XP_016878742.1:p.Gln93Ter
NM_001318193.2:c.253C>T	NP_001305122.2:p.Gln85Ter
NM_002528.7:c.253C>T MANE Select	NP_002519.2:p.Gln85Ter
NM_001318194.2:c.24+51C>T	NP_001305123.1:n.24+51C>T