Canonical Allele Identifier: CA340510584

Gene: C8B

Linked Data

• MyVariant Identifiers: chr1:g.57422498G>C (hg19) ; chr1:g.56956825G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.56956825G>C , CM000663.2:g.56956825G>C	GRCh38
NC_000001.10:g.57422498G>C , CM000663.1:g.57422498G>C	GRCh37
NC_000001.9:g.57195086G>C	NCBI36
NG_007285.1:g.14191C>G , LRG_31:g.14191C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468990.2:c.*176C>G	ENSP00000512215.1:n.*176C>G
ENST00000494324.2:c.*440C>G	ENSP00000512216.1:n.*440C>G
ENST00000695842.1:c.335C>G	ENSP00000512214.1:p.Thr112Ser
ENST00000695843.1:c.*176C>G	ENSP00000512217.1:n.*176C>G
ENST00000696144.1:c.335C>G	ENSP00000512436.1:p.Thr112Ser
ENST00000696164.1:c.335C>G	ENSP00000512454.1:p.Thr112Ser
ENST00000696165.1:c.*176C>G	ENSP00000512455.1:n.*176C>G
ENST00000696166.1:c.*176C>G	ENSP00000512456.1:n.*176C>G
ENST00000371237.9:c.335C>G MANE Select	ENSP00000360281.4:p.Thr112Ser
ENST00000371237.8:c.335C>G	ENSP00000360281.4:p.Thr112Ser
ENST00000535057.5:c.149C>G	ENSP00000440113.1:p.Thr50Ser
ENST00000543257.5:c.179C>G	ENSP00000442548.1:p.Thr60Ser
NM_000066.3:c.335C>G	NP_000057.2:p.Thr112Ser
NM_001278543.1:c.179C>G	NP_001265472.1:p.Thr60Ser
NM_001278544.1:c.149C>G	NP_001265473.1:p.Thr50Ser
XM_017002235.1:c.335C>G	XP_016857724.1:p.Thr112Ser
XR_001737397.1:n.435C>G
NM_000066.4:c.335C>G MANE Select	NP_000057.3:p.Thr112Ser
NM_001278543.2:c.179C>G	NP_001265472.2:p.Thr60Ser
NM_001278544.2:c.149C>G	NP_001265473.2:p.Thr50Ser