Canonical Allele Identifier: CA29294684
Gene: RAP1A HGNC NCBI

Linked Data

dbSNP Id: rs1031839208
MyVariant Identifiers: chr1:g.112107726G>A (hg19) chr1:g.111565104G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111565104G>A , CM000663.2:g.111565104G>A GRCh38
NC_000001.10:g.112107726G>A , CM000663.1:g.112107726G>A GRCh37
NC_000001.9:g.111909249G>A NCBI36
NG_032119.1:g.3872C>T , LRG_424:g.3872C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356415.5:c.-28+22595G>A ENSP00000348786.1:n.-28+22595G>A
XM_017001964.1:c.-28+22595G>A XP_016857453.1:n.-28+22595G>A
NM_001370216.1:c.-28+22595G>A NP_001357145.1:n.-28+22595G>A
NM_001370216.2:c.-28+22595G>A NP_001357145.1:n.-28+22595G>A
Search 100 bp 5'
Search 100 bp 3'