Canonical Allele Identifier: CA525494411
Gene: RAP1A HGNC NCBI

Linked Data

dbSNP Id: rs1399992792
gnomAD v2: 1-112107575-G-A
gnomAD v3: 1-111564953-G-A
gnomAD v4: 1-111564953-G-A
MyVariant Identifiers: chr1:g.112107575G>A (hg19) chr1:g.111564953G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111564953G>A , CM000663.2:g.111564953G>A GRCh38
NC_000001.10:g.112107575G>A , CM000663.1:g.112107575G>A GRCh37
NC_000001.9:g.111909098G>A NCBI36
NG_032119.1:g.4023C>T , LRG_424:g.4023C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356415.5:c.-28+22444G>A ENSP00000348786.1:n.-28+22444G>A
XM_017001964.1:c.-28+22444G>A XP_016857453.1:n.-28+22444G>A
NM_001370216.1:c.-28+22444G>A NP_001357145.1:n.-28+22444G>A
NM_001370216.2:c.-28+22444G>A NP_001357145.1:n.-28+22444G>A
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