Canonical Allele Identifier: CA292046617

Gene: RAD51C

Linked Data

• dbSNP Id: rs982832032
• gnomAD v2: 17-56769943-C-G
• gnomAD v3: 17-58692582-C-G
• gnomAD v4: 17-58692582-C-G
• MyVariant Identifiers: chr17:g.56769943C>G (hg19) ; chr17:g.58692582C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692582C>G , CM000679.2:g.58692582C>G	GRCh38
NC_000017.10:g.56769943C>G , CM000679.1:g.56769943C>G	GRCh37
NC_000017.9:g.54124942C>G	NCBI36
NG_023199.1:g.4981C>G , LRG_314:g.4981C>G
NG_047169.1:g.4498G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-310C>G	ENSP00000464056.2:n.-310C>G
ENST00000697675.1:n.10C>G
ENST00000697683.1:c.-62C>G	ENSP00000513395.1:n.-62C>G
ENST00000337432.8:c.-62C>G	ENSP00000336701.4:n.-62C>G
ENST00000461271.5:c.-310C>G	ENSP00000464056.1:n.-310C>G
ENST00000487921.5:n.7C>G
ENST00000583539.5:c.-62C>G	ENSP00000463121.1:n.-62C>G
NM_002876.3:c.-62C>G	NP_002867.1:n.-62C>G
NM_058216.2:c.-62C>G	NP_478123.1:n.-62C>G
NR_103872.1:n.10C>G
NR_103873.1:n.10C>G
XM_006722001.2:c.-62C>G	XP_006722064.1:n.-62C>G
XM_006722002.2:c.-62C>G	XP_006722065.1:n.-62C>G
XM_006722004.2:c.-310C>G	XP_006722067.1:n.-310C>G
XM_006722005.2:c.-257C>G	XP_006722068.1:n.-257C>G
XR_934513.1:n.12C>G
XR_934514.1:n.12C>G
XM_006722001.4:c.-62C>G	XP_006722064.1:n.-62C>G
XM_006722002.4:c.-62C>G	XP_006722065.1:n.-62C>G
XM_006722004.3:c.-310C>G	XP_006722067.1:n.-310C>G
XM_006722005.3:c.-257C>G	XP_006722068.1:n.-257C>G
XM_017024914.1:c.-310C>G	XP_016880403.1:n.-310C>G
XM_017024917.1:c.-257C>G	XP_016880406.1:n.-257C>G
XR_934513.3:n.443C>G
XR_934514.3:n.443C>G