Canonical Allele Identifier: CA174328334

Gene: NUGGC

Linked Data

• dbSNP Id: rs550745587
• gnomAD v3: 8-28065881-T-C
• gnomAD v4: 8-28065881-T-C
• MyVariant Identifiers: chr8:g.27923398T>C (hg19) ; chr8:g.28065881T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28065881T>C , CM000670.2:g.28065881T>C	GRCh38
NC_000008.10:g.27923398T>C , CM000670.1:g.27923398T>C	GRCh37
NC_000008.9:g.27979317T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000413272.7:c.712-1150A>G MANE Select	ENSP00000408697.2:n.712-1150A>G
ENST00000413272.6:c.712-1150A>G	ENSP00000408697.2:n.712-1150A>G
NM_001010906.1:c.712-1150A>G	NP_001010906.1:n.712-1150A>G
XM_011544523.1:c.784-1150A>G	XP_011542825.1:n.784-1150A>G
XM_011544524.1:c.784-1150A>G	XP_011542826.1:n.784-1150A>G
XM_011544526.1:c.784-1150A>G	XP_011542828.1:n.784-1150A>G
XM_011544523.2:c.784-1150A>G	XP_011542825.1:n.784-1150A>G
XM_011544524.3:c.784-1150A>G	XP_011542826.1:n.784-1150A>G
XM_011544526.2:c.784-1150A>G	XP_011542828.1:n.784-1150A>G
XM_017013403.1:c.784-1150A>G	XP_016868892.1:n.784-1150A>G
NM_001010906.2:c.712-1150A>G MANE Select	NP_001010906.1:n.712-1150A>G