Canonical Allele Identifier: CA29294680

Gene: RAP1A

Linked Data

• dbSNP Id: rs906940687
• gnomAD v2: 1-112107709-T-C
• gnomAD v3: 1-111565087-T-C
• gnomAD v4: 1-111565087-T-C
• MyVariant Identifiers: chr1:g.112107709T>C (hg19) ; chr1:g.111565087T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111565087T>C , CM000663.2:g.111565087T>C	GRCh38
NC_000001.10:g.112107709T>C , CM000663.1:g.112107709T>C	GRCh37
NC_000001.9:g.111909232T>C	NCBI36
NG_032119.1:g.3889A>G , LRG_424:g.3889A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356415.5:c.-28+22578T>C	ENSP00000348786.1:n.-28+22578T>C
XM_017001964.1:c.-28+22578T>C	XP_016857453.1:n.-28+22578T>C
NM_001370216.1:c.-28+22578T>C	NP_001357145.1:n.-28+22578T>C
NM_001370216.2:c.-28+22578T>C	NP_001357145.1:n.-28+22578T>C