Canonical Allele Identifier: CA2792527954

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036417C>T , CM000673.2:g.68036417C>T	GRCh38
NC_000011.9:g.67803884C>T , CM000673.1:g.67803884C>T	GRCh37
NC_000011.8:g.67560460C>T	NCBI36
NG_007878.1:g.2402C>T , LRG_115:g.2402C>T
NG_017040.1:g.10801C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.501+36C>T MANE Select	ENSP00000315774.5:n.501+36C>T
ENST00000313468.9:c.501+36C>T	ENSP00000315774.5:n.501+36C>T
ENST00000524810.5:c.433+36C>T
ENST00000526339.5:c.501+36C>T	ENSP00000436287.1:n.501+36C>T
ENST00000526446.5:c.*556+36C>T	ENSP00000433645.1:n.*556+36C>T
ENST00000528492.1:c.63+36C>T	ENSP00000432848.1:n.63+36C>T
ENST00000531282.1:n.353+36C>T
NM_002496.3:c.501+36C>T	NP_002487.1:n.501+36C>T
XM_005274013.1:c.501+36C>T	XP_005274070.1:n.501+36C>T
XM_005274014.1:c.501+36C>T	XP_005274071.1:n.501+36C>T
XM_005274015.1:c.381+36C>T	XP_005274072.1:n.381+36C>T
XM_011545053.1:c.501+36C>T	XP_011543355.1:n.501+36C>T
NM_002496.4:c.501+36C>T MANE Select	NP_002487.1:n.501+36C>T