Canonical Allele Identifier: CA292046611

Gene: RAD51C

Linked Data

• dbSNP Id: rs952662506
• gnomAD v2: 17-56769938-T-C
• gnomAD v3: 17-58692577-T-C
• gnomAD v4: 17-58692577-T-C
• MyVariant Identifiers: chr17:g.56769938T>C (hg19) ; chr17:g.58692577T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692577T>C , CM000679.2:g.58692577T>C	GRCh38
NC_000017.10:g.56769938T>C , CM000679.1:g.56769938T>C	GRCh37
NC_000017.9:g.54124937T>C	NCBI36
NG_023199.1:g.4976T>C , LRG_314:g.4976T>C
NG_047169.1:g.4503A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-315T>C	ENSP00000464056.2:n.-315T>C
ENST00000697675.1:n.5T>C
ENST00000337432.8:c.-67T>C	ENSP00000336701.4:n.-67T>C
ENST00000461271.5:c.-315T>C	ENSP00000464056.1:n.-315T>C
ENST00000487921.5:n.2T>C
ENST00000583539.5:c.-67T>C	ENSP00000463121.1:n.-67T>C
NM_002876.3:c.-67T>C	NP_002867.1:n.-67T>C
NM_058216.2:c.-67T>C	NP_478123.1:n.-67T>C
NR_103872.1:n.5T>C
NR_103873.1:n.5T>C
XM_006722001.2:c.-67T>C	XP_006722064.1:n.-67T>C
XM_006722002.2:c.-67T>C	XP_006722065.1:n.-67T>C
XM_006722004.2:c.-315T>C	XP_006722067.1:n.-315T>C
XM_006722005.2:c.-262T>C	XP_006722068.1:n.-262T>C
XR_934513.1:n.7T>C
XR_934514.1:n.7T>C
XM_006722001.4:c.-67T>C	XP_006722064.1:n.-67T>C
XM_006722002.4:c.-67T>C	XP_006722065.1:n.-67T>C
XM_006722004.3:c.-315T>C	XP_006722067.1:n.-315T>C
XM_006722005.3:c.-262T>C	XP_006722068.1:n.-262T>C
XM_017024914.1:c.-315T>C	XP_016880403.1:n.-315T>C
XM_017024917.1:c.-262T>C	XP_016880406.1:n.-262T>C
XR_934513.3:n.438T>C
XR_934514.3:n.438T>C