Canonical Allele Identifier: CA1049071718

Gene: SUCLG2

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.67401619C>G , CM000665.2:g.67401619C>G	GRCh38
NC_000003.11:g.67452043C>G , CM000665.1:g.67452043C>G	GRCh37
NC_000003.10:g.67534733C>G	NCBI36
NG_052945.1:g.257996G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307227.10:c.1063-768G>C MANE Select	ENSP00000307432.5:n.1063-768G>C
ENST00000307227.9:c.1063-768G>C	ENSP00000307432.5:n.1063-768G>C
ENST00000460567.5:c.335-768G>C
ENST00000493112.5:c.1063-768G>C	ENSP00000419325.1:n.1063-768G>C
NM_001177599.1:c.1063-768G>C	NP_001171070.1:n.1063-768G>C
NM_003848.3:c.1063-768G>C	NP_003839.2:n.1063-768G>C
XR_245062.2:n.1087-768G>C
XR_940506.1:n.1257-768G>C
XM_017007420.2:c.1063-768G>C	XP_016862909.1:n.1063-768G>C
XR_001740348.2:n.1258-768G>C
NM_001177599.2:c.1063-768G>C	NP_001171070.1:n.1063-768G>C
NM_003848.4:c.1063-768G>C MANE Select	NP_003839.2:n.1063-768G>C