Canonical Allele Identifier: CA2688143412

Gene: RRM2B

Linked Data

• gnomAD v4: 8-102208052-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208052C>A , CM000670.2:g.102208052C>A	GRCh38
NC_000008.10:g.103220280C>A , CM000670.1:g.103220280C>A	GRCh37
NC_000008.9:g.103289456C>A	NCBI36
NG_016617.1:g.36067G>T , LRG_788:g.36067G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.*81G>T MANE Select	ENSP00000251810.3:n.*81G>T
ENST00000251810.7:c.*81G>T	ENSP00000251810.3:n.*81G>T
ENST00000395910.6:n.524G>T
ENST00000522368.5:c.1306G>T
ENST00000621845.1:c.*81G>T	ENSP00000484318.1:n.*81G>T
NM_001172477.1:c.*81G>T , LRG_788t1:c.*81G>T	NP_001165948.1:n.*81G>T
NM_001172478.1:c.*81G>T	NP_001165949.1:n.*81G>T
NM_015713.4:c.*81G>T , LRG_788t2:c.*81G>T	NP_056528.2:n.*81G>T
NM_001172478.2:c.*81G>T	NP_001165949.1:n.*81G>T
NM_015713.5:c.*81G>T MANE Select	NP_056528.2:n.*81G>T