Canonical Allele Identifier: CA1619136576
Gene: MICA HGNC NCBI

Linked Data

dbSNP Id: rs1770524796

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31403012A>T , CM000668.2:g.31403012A>T GRCh38
NC_000006.11:g.31370789A>T , CM000668.1:g.31370789A>T GRCh37
NC_000006.10:g.31478768A>T NCBI36
NG_034139.1:g.8229A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000667609.1:n.920A>T
ENST00000673647.1:c.-188-433A>T ENSP00000500967.1:n.-188-433A>T
ENST00000673996.1:n.79+2229A>T
ENST00000674069.1:c.-173+2249A>T ENSP00000501157.1:n.-173+2249A>T
ENST00000674131.1:c.-188-433A>T ENSP00000501002.1:n.-188-433A>T
ENST00000616296.4:c.-222+2229A>T ENSP00000482382.1:n.-222+2229A>T
NM_001289152.1:c.-222+2229A>T NP_001276081.1:n.-222+2229A>T
NM_001289153.1:c.-222+2249A>T NP_001276082.1:n.-222+2249A>T
NM_001289154.1:c.-173+2249A>T NP_001276083.1:n.-173+2249A>T
NM_001289152.2:c.-222+2229A>T NP_001276081.1:n.-222+2229A>T
NM_001289153.2:c.-222+2249A>T NP_001276082.1:n.-222+2249A>T
NM_001289154.2:c.-173+2249A>T NP_001276083.1:n.-173+2249A>T