Canonical Allele Identifier: CA1188974197

Gene: RAP1A

Linked Data

• dbSNP Id: rs1296902989

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.111564958T>G , CM000663.2:g.111564958T>G	GRCh38
NC_000001.10:g.112107580T>G , CM000663.1:g.112107580T>G	GRCh37
NC_000001.9:g.111909103T>G	NCBI36
NG_032119.1:g.4018A>C , LRG_424:g.4018A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356415.5:c.-28+22449T>G	ENSP00000348786.1:n.-28+22449T>G
XM_017001964.1:c.-28+22449T>G	XP_016857453.1:n.-28+22449T>G
NM_001370216.1:c.-28+22449T>G	NP_001357145.1:n.-28+22449T>G
NM_001370216.2:c.-28+22449T>G	NP_001357145.1:n.-28+22449T>G