Canonical Allele Identifier: CA844776826

Gene: RRM2B

Linked Data

• dbSNP Id: rs1192939468
• gnomAD v3: 8-102238927-C-A
• gnomAD v4: 8-102238927-C-A
• MyVariant Identifiers: chr8:g.103251155C>A (hg19) ; chr8:g.102238927C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102238927C>A , CM000670.2:g.102238927C>A	GRCh38
NC_000008.10:g.103251155C>A , CM000670.1:g.103251155C>A	GRCh37
NC_000008.9:g.103320331C>A	NCBI36
NG_016617.1:g.5192G>T , LRG_788:g.5192G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.-53G>T MANE Select	ENSP00000251810.3:n.-53G>T
ENST00000251810.7:c.-53G>T	ENSP00000251810.3:n.-53G>T
ENST00000523957.1:c.-53G>T	ENSP00000427830.1:n.-53G>T
NM_001172478.1:c.-53G>T	NP_001165949.1:n.-53G>T
NM_015713.4:c.-53G>T , LRG_788t2:c.-53G>T	NP_056528.2:n.-53G>T
NM_001172478.2:c.-53G>T	NP_001165949.1:n.-53G>T
NM_015713.5:c.-53G>T MANE Select	NP_056528.2:n.-53G>T