Canonical Allele Identifier: CA371586124

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220462C>A (hg19) ; chr8:g.102208234C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208234C>A , CM000670.2:g.102208234C>A	GRCh38
NC_000008.10:g.103220462C>A , CM000670.1:g.103220462C>A	GRCh37
NC_000008.9:g.103289638C>A	NCBI36
NG_016617.1:g.35885G>T , LRG_788:g.35885G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.955G>T MANE Select	ENSP00000251810.3:p.Gly319Ter
ENST00000251810.7:c.955G>T	ENSP00000251810.3:p.Gly319Ter
ENST00000395910.6:n.342G>T
ENST00000395912.6:c.799G>T	ENSP00000379248.2:p.Gly267Ter
ENST00000519317.5:c.319G>T	ENSP00000430641.1:p.Gly107Ter
ENST00000519962.5:c.100G>T	ENSP00000429140.1:p.Gly34Ter
ENST00000522368.5:c.1124G>T
ENST00000522394.1:c.288G>T	ENSP00000429578.1:n.288G>T
ENST00000621845.1:c.793G>T	ENSP00000484318.1:p.Gly265Ter
NM_001172477.1:c.1171G>T , LRG_788t1:c.1171G>T	NP_001165948.1:p.Gly391Ter
NM_001172478.1:c.799G>T	NP_001165949.1:p.Gly267Ter
NM_015713.4:c.955G>T , LRG_788t2:c.955G>T	NP_056528.2:p.Gly319Ter
NM_001172478.2:c.799G>T	NP_001165949.1:p.Gly267Ter
NM_015713.5:c.955G>T MANE Select	NP_056528.2:p.Gly319Ter