Canonical Allele Identifier: CA4830955

Gene: RRM2B

Linked Data

• dbSNP Id: rs202129216
• ExAC: 8:103220356 G / A
• gnomAD v2: 8-103220356-G-A
• gnomAD v3: 8-102208128-G-A
• gnomAD v4: 8-102208128-G-A
• MyVariant Identifiers: chr8:g.103220356G>A (hg19) ; chr8:g.102208128G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208128G>A , CM000670.2:g.102208128G>A	GRCh38
NC_000008.10:g.103220356G>A , CM000670.1:g.103220356G>A	GRCh37
NC_000008.9:g.103289532G>A	NCBI36
NG_016617.1:g.35991C>T , LRG_788:g.35991C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.*5C>T MANE Select	ENSP00000251810.3:n.*5C>T
ENST00000251810.7:c.*5C>T	ENSP00000251810.3:n.*5C>T
ENST00000395910.6:n.448C>T
ENST00000522368.5:c.1230C>T
ENST00000621845.1:c.*5C>T	ENSP00000484318.1:n.*5C>T
NM_001172477.1:c.*5C>T , LRG_788t1:c.*5C>T	NP_001165948.1:n.*5C>T
NM_001172478.1:c.*5C>T	NP_001165949.1:n.*5C>T
NM_015713.4:c.*5C>T , LRG_788t2:c.*5C>T	NP_056528.2:n.*5C>T
NM_001172478.2:c.*5C>T	NP_001165949.1:n.*5C>T
NM_015713.5:c.*5C>T MANE Select	NP_056528.2:n.*5C>T