Canonical Allele Identifier: CA525494400
Gene: RAP1A HGNC NCBI

Linked Data

dbSNP Id: rs1168066282
gnomAD v2: 1-112107501-A-T
gnomAD v3: 1-111564879-A-T
gnomAD v4: 1-111564879-A-T
MyVariant Identifiers: chr1:g.112107501A>T (hg19) chr1:g.111564879A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111564879A>T , CM000663.2:g.111564879A>T GRCh38
NC_000001.10:g.112107501A>T , CM000663.1:g.112107501A>T GRCh37
NC_000001.9:g.111909024A>T NCBI36
NG_032119.1:g.4097T>A , LRG_424:g.4097T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356415.5:c.-28+22370A>T ENSP00000348786.1:n.-28+22370A>T
XM_017001964.1:c.-28+22370A>T XP_016857453.1:n.-28+22370A>T
NM_001370216.1:c.-28+22370A>T NP_001357145.1:n.-28+22370A>T
NM_001370216.2:c.-28+22370A>T NP_001357145.1:n.-28+22370A>T
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