Canonical Allele Identifier: CA15659876
Gene: ARMH3 HGNC NCBI

Linked Data

dbSNP Id: rs34014631
gnomAD v2: 10-103698705-G-A
gnomAD v3: 10-101938948-G-A
gnomAD v4: 10-101938948-G-A
MyVariant Identifiers: chr10:g.103698705G>A (hg19) chr10:g.101938948G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101938948G>A , CM000672.2:g.101938948G>A GRCh38
NC_000010.10:g.103698705G>A , CM000672.1:g.103698705G>A GRCh37
NC_000010.9:g.103688695G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370033.9:c.1781+915C>T MANE Select ENSP00000359050.4:n.1781+915C>T
ENST00000370033.8:c.1781+915C>T ENSP00000359050.4:n.1781+915C>T
NM_024541.2:c.1781+915C>T NP_078817.2:n.1781+915C>T
XM_006717969.1:c.1571+915C>T XP_006718032.1:n.1571+915C>T
XM_011540151.1:c.1781+915C>T XP_011538453.1:n.1781+915C>T
XM_011540152.1:c.1715+915C>T XP_011538454.1:n.1715+915C>T
XM_011540153.1:c.1679+915C>T XP_011538455.1:n.1679+915C>T
XM_011540154.1:c.1613+915C>T XP_011538456.1:n.1613+915C>T
XM_011540155.1:c.1781+915C>T XP_011538457.1:n.1781+915C>T
XM_011540156.1:c.1259+915C>T XP_011538458.1:n.1259+915C>T
XM_011540157.1:c.1628+915C>T XP_011538459.1:n.1628+915C>T
XR_246104.2:n.1881+915C>T
XM_011540151.3:c.1781+915C>T XP_011538453.1:n.1781+915C>T
XM_011540152.2:c.1715+915C>T XP_011538454.1:n.1715+915C>T
XM_011540153.2:c.1679+915C>T XP_011538455.1:n.1679+915C>T
XM_011540154.2:c.1613+915C>T XP_011538456.1:n.1613+915C>T
XM_011540156.2:c.1259+915C>T XP_011538458.1:n.1259+915C>T
XM_011540157.2:c.1628+915C>T XP_011538459.1:n.1628+915C>T
XM_017016635.1:c.1781+915C>T XP_016872124.1:n.1781+915C>T
XM_017016636.2:c.1781+915C>T XP_016872125.1:n.1781+915C>T
XR_001747199.1:n.1881+915C>T
XR_001747200.1:n.1805+17649C>T
XR_001747201.1:n.2360+915C>T
XR_001747202.1:n.1999+915C>T
NM_024541.3:c.1781+915C>T MANE Select NP_078817.2:n.1781+915C>T
Search 100 bp 5'
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