Canonical Allele Identifier: CA850468165

Gene: NUGGC

Linked Data

• dbSNP Id: rs1471438539
• MyVariant Identifiers: chr8:g.27923570G>A (hg19) ; chr8:g.28066053G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28066053G>A , CM000670.2:g.28066053G>A	GRCh38
NC_000008.10:g.27923570G>A , CM000670.1:g.27923570G>A	GRCh37
NC_000008.9:g.27979489G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413272.7:c.712-1322C>T MANE Select	ENSP00000408697.2:n.712-1322C>T
ENST00000413272.6:c.712-1322C>T	ENSP00000408697.2:n.712-1322C>T
NM_001010906.1:c.712-1322C>T	NP_001010906.1:n.712-1322C>T
XM_011544523.1:c.784-1322C>T	XP_011542825.1:n.784-1322C>T
XM_011544524.1:c.784-1322C>T	XP_011542826.1:n.784-1322C>T
XM_011544526.1:c.784-1322C>T	XP_011542828.1:n.784-1322C>T
XM_011544523.2:c.784-1322C>T	XP_011542825.1:n.784-1322C>T
XM_011544524.3:c.784-1322C>T	XP_011542826.1:n.784-1322C>T
XM_011544526.2:c.784-1322C>T	XP_011542828.1:n.784-1322C>T
XM_017013403.1:c.784-1322C>T	XP_016868892.1:n.784-1322C>T
NM_001010906.2:c.712-1322C>T MANE Select	NP_001010906.1:n.712-1322C>T