Canonical Allele Identifier: CA455894580

Gene: NCF1

Linked Data

• dbSNP Id: rs782794682
• MyVariant Identifiers: chr7:g.74197950G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.74783607G>C , CM000669.2:g.74783607G>C	GRCh38
NC_000007.13:g.74197950G>C , CM000669.1:g.74197950G>C	GRCh37
NC_000007.12:g.73835886G>C	NCBI36
NG_009078.2:g.14644G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289473.11:c.657G>C MANE Select	ENSP00000289473.4:p.Thr219=
ENST00000289473.10:c.657G>C	ENSP00000289473.4:p.Thr219=
ENST00000289473.8:c.657G>C	ENSP00000289473.4:p.Thr219=
ENST00000398421.6:n.1214G>C
ENST00000443956.7:n.778G>C
ENST00000455062.2:n.804G>C
ENST00000486097.1:n.165G>C
NM_000265.5:c.657G>C	NP_000256.4:p.Thr219=
XM_005250543.3:c.657G>C	XP_005250600.2:p.Thr219=
XM_005250544.3:c.657G>C	XP_005250601.2:p.Thr219=
XM_011516498.1:c.657G>C	XP_011514800.1:p.Thr219=
XM_011516499.1:c.657G>C	XP_011514801.1:p.Thr219=
XM_011516500.1:c.657G>C	XP_011514802.1:p.Thr219=
XM_011516501.1:c.264G>C	XP_011514803.1:p.Thr88=
XR_242262.3:n.712G>C
XR_927515.1:n.712G>C
NM_000265.6:c.657G>C	NP_000256.4:p.Thr219=
NM_000265.7:c.657G>C MANE Select	NP_000256.4:p.Thr219=