Canonical Allele Identifier: CA15250787

Gene: SUCLG2

Linked Data

• dbSNP Id: rs6792584
• gnomAD v2: 3-67531388-G-A
• gnomAD v3: 3-67480964-G-A
• gnomAD v4: 3-67480964-G-A
• MyVariant Identifiers: chr3:g.67531388G>A (hg19) ; chr3:g.67480964G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.67480964G>A , CM000665.2:g.67480964G>A	GRCh38
NC_000003.11:g.67531388G>A , CM000665.1:g.67531388G>A	GRCh37
NC_000003.10:g.67614078G>A	NCBI36
NG_052945.1:g.178651C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000307227.10:c.1062+14834C>T MANE Select	ENSP00000307432.5:n.1062+14834C>T
ENST00000307227.9:c.1062+14834C>T	ENSP00000307432.5:n.1062+14834C>T
ENST00000460567.5:c.334+37283C>T
ENST00000492795.1:c.1062+14834C>T	ENSP00000417589.1:n.1062+14834C>T
ENST00000493112.5:c.1062+14834C>T	ENSP00000419325.1:n.1062+14834C>T
NM_001177599.1:c.1062+14834C>T	NP_001171070.1:n.1062+14834C>T
NM_003848.3:c.1062+14834C>T	NP_003839.2:n.1062+14834C>T
XR_245062.2:n.1086+14834C>T
XR_940506.1:n.1086+14834C>T
XM_017007420.2:c.1062+14834C>T	XP_016862909.1:n.1062+14834C>T
XR_001740348.2:n.1087+14834C>T
XR_001740350.2:n.1087+14834C>T
NM_001177599.2:c.1062+14834C>T	NP_001171070.1:n.1062+14834C>T
NM_003848.4:c.1062+14834C>T MANE Select	NP_003839.2:n.1062+14834C>T