Canonical Allele Identifier: CA15183310
Gene: RAMP1 HGNC NCBI

Linked Data

dbSNP Id: rs3769048
gnomAD v2: 2-238769861-G-A
gnomAD v3: 2-237861218-G-A
gnomAD v4: 2-237861218-G-A
MyVariant Identifiers: chr2:g.238769861G>A (hg19) chr2:g.237861218G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237861218G>A , CM000664.2:g.237861218G>A GRCh38
NC_000002.11:g.238769861G>A , CM000664.1:g.238769861G>A GRCh37
NC_000002.10:g.238434600G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000254661.5:c.52+1491G>A MANE Select ENSP00000254661.4:n.52+1491G>A
ENST00000254661.4:c.52+1491G>A ENSP00000254661.4:n.52+1491G>A
ENST00000403885.1:c.-15+1215G>A ENSP00000386046.1:n.-15+1215G>A
ENST00000404910.6:c.-15+2091G>A ENSP00000384688.2:n.-15+2091G>A
ENST00000409726.5:c.-76+1491G>A ENSP00000386720.1:n.-76+1491G>A
NM_001308353.1:c.-76+1491G>A NP_001295282.1:n.-76+1491G>A
NM_005855.2:c.52+1491G>A NP_005846.1:n.52+1491G>A
NM_005855.3:c.52+1491G>A NP_005846.1:n.52+1491G>A
XM_011510478.1:c.-182+1011G>A XP_011508780.1:n.-182+1011G>A
XM_017003152.2:c.-15+1215G>A XP_016858641.1:n.-15+1215G>A
XM_017003153.2:c.-15+2091G>A XP_016858642.1:n.-15+2091G>A
XM_017003155.1:c.52+1491G>A XP_016858644.1:n.52+1491G>A
XM_017003156.2:c.-15+1011G>A XP_016858645.1:n.-15+1011G>A
NM_005855.4:c.52+1491G>A MANE Select NP_005846.1:n.52+1491G>A
NM_001308353.2:c.-76+1491G>A NP_001295282.1:n.-76+1491G>A
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