Canonical Allele Identifier: CA2673689365

Gene: C7

Linked Data

• gnomAD v4: 5-40979645-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.40979645A>T , CM000667.2:g.40979645A>T	GRCh38
NC_000005.9:g.40979747A>T , CM000667.1:g.40979747A>T	GRCh37
NC_000005.8:g.41015504A>T	NCBI36
NG_011692.1:g.75149A>T , LRG_30:g.75149A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696333.1:c.2166-80A>T	ENSP00000512566.1:n.2166-80A>T
ENST00000696441.1:c.2166-80A>T	ENSP00000512631.1:n.2166-80A>T
ENST00000696442.1:n.100-80A>T
ENST00000706664.1:n.2280-80A>T
ENST00000706666.1:n.2241+2805A>T
ENST00000706667.1:n.3056-80A>T
ENST00000706668.1:n.2894-80A>T
ENST00000313164.10:c.2166-80A>T MANE Select	ENSP00000322061.9:n.2166-80A>T
ENST00000313164.9:c.2166-80A>T	ENSP00000322061.9:n.2166-80A>T
ENST00000464864.1:n.179-80A>T
ENST00000494960.5:n.166-80A>T
NM_000587.2:c.2166-80A>T , LRG_30t1:c.2166-80A>T	NP_000578.2:n.2166-80A>T
XM_011514122.1:c.2166-80A>T	XP_011512424.1:n.2166-80A>T
NM_000587.3:c.2166-80A>T	NP_000578.2:n.2166-80A>T
NM_000587.4:c.2166-80A>T MANE Select	NP_000578.2:n.2166-80A>T