Canonical Allele Identifier: CA292994722
Gene: MILR1 HGNC NCBI

Linked Data

dbSNP Id: rs12936887
MyVariant Identifiers: chr17:g.64462382A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.64462382A>G , CM000679.2:g.64462382A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000619286.5:c.763+1450A>G MANE Select ENSP00000482801.1:n.763+1450A>G
ENST00000612535.4:c.493+1450A>G ENSP00000477504.1:n.493+1450A>G
ENST00000615220.4:c.763+1450A>G ENSP00000480749.1:n.763+1450A>G
ENST00000616498.4:c.478+1450A>G ENSP00000481318.1:n.478+1450A>G
ENST00000619286.4:c.763+1450A>G ENSP00000482801.1:n.763+1450A>G
NM_001085423.1:c.763+1450A>G NP_001078892.1:n.763+1450A>G
NM_001291316.1:c.478+1450A>G NP_001278245.1:n.478+1450A>G
NM_001291317.1:c.493+1450A>G NP_001278246.1:n.493+1450A>G
XM_005276872.3:c.889+1450A>G XP_005276929.1:n.889+1450A>G
XM_005276874.3:c.889+1450A>G XP_005276931.1:n.889+1450A>G
XM_005276875.3:c.889+1450A>G XP_005276932.1:n.889+1450A>G
XM_005276876.3:c.889+1450A>G XP_005276933.1:n.889+1450A>G
XM_005276877.3:c.604+1450A>G XP_005276934.1:n.604+1450A>G
XM_005276878.2:c.589+1450A>G XP_005276935.1:n.589+1450A>G
XM_011524627.1:c.889+1450A>G XP_011522929.1:n.889+1450A>G
XM_017024486.1:c.889+1450A>G XP_016879975.1:n.889+1450A>G
XM_017024487.1:c.589+1450A>G XP_016879976.1:n.589+1450A>G
XM_024450706.1:c.889+1450A>G XP_024306474.1:n.889+1450A>G
XM_024450707.1:c.889+1450A>G XP_024306475.1:n.889+1450A>G
XM_024450708.1:c.889+1450A>G XP_024306476.1:n.889+1450A>G
XM_024450709.1:c.889+1450A>G XP_024306477.1:n.889+1450A>G
XR_002957989.1:n.910+1450A>G
XR_002957990.1:n.910+1450A>G
NM_001085423.2:c.763+1450A>G MANE Select NP_001078892.1:n.763+1450A>G
NM_001291316.2:c.478+1450A>G NP_001278245.1:n.478+1450A>G
NM_001291317.2:c.493+1450A>G NP_001278246.1:n.493+1450A>G
NM_001369493.1:c.763+1450A>G NP_001356422.1:n.763+1450A>G