Canonical Allele Identifier: CA242785464

Gene: C12orf42

Linked Data

• dbSNP Id: rs10778213
• gnomAD v2: 12-103495151-T-C
• gnomAD v3: 12-103101373-T-C
• gnomAD v4: 12-103101373-T-C
• MyVariant Identifiers: chr12:g.103495151T>C (hg19) ; chr12:g.103101373T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.103101373T>C , CM000674.2:g.103101373T>C	GRCh38
NC_000012.11:g.103495151T>C , CM000674.1:g.103495151T>C	GRCh37
NC_000012.10:g.102019281T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011538310.1:c.*22-19836A>G	XP_011536612.1:n.*22-19836A>G
XR_001748690.1:n.665-53047A>G
NM_001386867.1:c.*22-19836A>G	NP_001373796.1:n.*22-19836A>G
NR_170336.1:n.1120-19836A>G