Canonical Allele Identifier: CA1087457583
Gene: MICA HGNC NCBI

Linked Data

dbSNP Id: rs1770517948
gnomAD v3: 6-31402912-G-C
gnomAD v4: 6-31402912-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31402912G>C , CM000668.2:g.31402912G>C GRCh38
NC_000006.11:g.31370689G>C , CM000668.1:g.31370689G>C GRCh37
NC_000006.10:g.31478668G>C NCBI36
NG_034139.1:g.8129G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000667609.1:n.820G>C
ENST00000673647.1:c.-188-533G>C ENSP00000500967.1:n.-188-533G>C
ENST00000673996.1:n.79+2129G>C
ENST00000674069.1:c.-173+2149G>C ENSP00000501157.1:n.-173+2149G>C
ENST00000674131.1:c.-188-533G>C ENSP00000501002.1:n.-188-533G>C
ENST00000616296.4:c.-222+2129G>C ENSP00000482382.1:n.-222+2129G>C
NM_001289152.1:c.-222+2129G>C NP_001276081.1:n.-222+2129G>C
NM_001289153.1:c.-222+2149G>C NP_001276082.1:n.-222+2149G>C
NM_001289154.1:c.-173+2149G>C NP_001276083.1:n.-173+2149G>C
NM_001289152.2:c.-222+2129G>C NP_001276081.1:n.-222+2129G>C
NM_001289153.2:c.-222+2149G>C NP_001276082.1:n.-222+2149G>C
NM_001289154.2:c.-173+2149G>C NP_001276083.1:n.-173+2149G>C