Canonical Allele Identifier: CA1365911
Gene: FCAMR HGNC NCBI

Linked Data

dbSNP Id: rs1856746
ExAC: 1:207143422 A / G
gnomAD v2: 1-207143422-A-G
gnomAD v3: 1-206970077-A-G
gnomAD v4: 1-206970077-A-G
MyVariant Identifiers: chr1:g.207143422A>G (hg19) chr1:g.206970077A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206970077A>G , CM000663.2:g.206970077A>G GRCh38
NC_000001.10:g.207143422A>G , CM000663.1:g.207143422A>G GRCh37
NC_000001.9:g.205210045A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000324852.9:c.39+10T>C MANE Select ENSP00000316491.4:n.39+10T>C
ENST00000400962.8:c.39+10T>C ENSP00000383746.3:n.39+10T>C
ENST00000450945.3:c.39+10T>C ENSP00000392707.2:n.39+10T>C
ENST00000324852.8:c.39+10T>C ENSP00000316491.4:n.39+10T>C
ENST00000324863.6:c.39+10T>C ENSP00000317155.2:n.39+10T>C
ENST00000400962.7:c.39+10T>C ENSP00000383746.3:n.39+10T>C
ENST00000450945.2:c.39+10T>C ENSP00000392707.2:n.39+10T>C
ENST00000487149.5:n.313+10T>C
ENST00000488345.1:n.414+10T>C
NM_001122979.2:c.39+10T>C NP_001116451.1:n.39+10T>C
NM_001170631.1:c.39+10T>C NP_001164102.1:n.39+10T>C
NM_032029.4:c.39+10T>C NP_114418.2:n.39+10T>C
XM_011510051.1:c.39+10T>C XP_011508353.1:n.39+10T>C
XM_011510051.2:c.39+10T>C XP_011508353.1:n.39+10T>C
XM_017002442.1:c.39+10T>C XP_016857931.1:n.39+10T>C
NM_001170631.2:c.39+10T>C MANE Select NP_001164102.1:n.39+10T>C
NM_001122979.3:c.39+10T>C NP_001116451.1:n.39+10T>C
NM_032029.5:c.39+10T>C NP_114418.2:n.39+10T>C
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