Canonical Allele Identifier: CA199379987

Gene: C5

Linked Data

• dbSNP Id: rs952164906
• gnomAD v2: 9-123716811-C-G
• gnomAD v3: 9-120954533-C-G
• gnomAD v4: 9-120954533-C-G
• MyVariant Identifiers: chr9:g.123716811C>G (hg19) ; chr9:g.120954533C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120954533C>G , CM000671.2:g.120954533C>G	GRCh38
NC_000009.11:g.123716811C>G , CM000671.1:g.123716811C>G	GRCh37
NC_000009.10:g.122756632C>G	NCBI36
NG_007364.1:g.100744G>C , LRG_28:g.100744G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000480188.2:n.4548G>C
ENST00000696279.1:c.5083-665G>C
ENST00000696280.1:n.4852-665G>C
ENST00000696281.1:c.4781-665G>C	ENSP00000512521.1:n.4781-665G>C
ENST00000697921.1:n.3641-665G>C
ENST00000697922.1:c.*4753-665G>C	ENSP00000513478.1:n.*4753-665G>C
ENST00000697923.1:n.7959G>C
ENST00000223642.3:c.4763-665G>C MANE Select	ENSP00000223642.1:n.4763-665G>C
ENST00000223642.2:c.4763-665G>C	ENSP00000223642.1:n.4763-665G>C
NM_001735.2:c.4763-665G>C , LRG_28t1:c.4763-665G>C	NP_001726.2:n.4763-665G>C
XM_011518980.1:c.4778-665G>C	XP_011517282.1:n.4778-665G>C
NM_001317163.1:c.4781-665G>C	NP_001304092.1:n.4781-665G>C
NM_001317163.2:c.4781-665G>C	NP_001304092.1:n.4781-665G>C
NM_001735.3:c.4763-665G>C MANE Select	NP_001726.2:n.4763-665G>C