Canonical Allele Identifier: CA127037
Gene: C8A HGNC NCBI

Linked Data

ClinVar Variation Id: 17039
dbSNP Id: rs652785
gnomAD v2: 1-57340727-C-A
gnomAD v3: 1-56875054-C-A
gnomAD v4: 1-56875054-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56875054C>A , CM000663.2:g.56875054C>A GRCh38
NC_000001.10:g.57340727C>A , CM000663.1:g.57340727C>A GRCh37
NC_000001.9:g.57113315C>A NCBI36
NG_012049.1:g.25285C>A , LRG_139:g.25285C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695676.1:n.411C>A
ENST00000695677.1:c.277C>A ENSP00000512097.1:p.Gln93Lys
ENST00000695678.1:c.277C>A ENSP00000512098.1:p.Gln93Lys
ENST00000695679.1:c.277C>A ENSP00000512099.1:p.Gln93Lys
ENST00000695680.1:n.383C>A
ENST00000695681.1:c.277C>A ENSP00000512100.1:p.Gln93Lys
ENST00000695682.1:n.371C>A
ENST00000695683.1:n.308C>A
ENST00000695684.1:n.175C>A
ENST00000695685.1:n.228C>A
ENST00000695723.1:c.277C>A ENSP00000512121.1:p.Gln93Lys
ENST00000361249.4:c.277C>A MANE Select ENSP00000354458.3:p.Gln93Lys
ENST00000361249.3:c.277C>A ENSP00000354458.3:p.Gln93Lys
NM_000562.2:c.277C>A , LRG_139t1:c.277C>A NP_000553.1:p.Gln93Lys
XM_011542079.1:c.277C>A XP_011540381.1:p.Gln93Lys
XM_011542079.2:c.277C>A XP_011540381.1:p.Gln93Lys
XM_017002234.1:c.277C>A XP_016857723.1:p.Gln93Lys
NM_000562.3:c.277C>A MANE Select NP_000553.1:p.Gln93Lys