Canonical Allele Identifier: CA1619136307
Gene: MICA HGNC NCBI

Linked Data

dbSNP Id: rs1770477806

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31402372A>G , CM000668.2:g.31402372A>G GRCh38
NC_000006.11:g.31370149A>G , CM000668.1:g.31370149A>G GRCh37
NC_000006.10:g.31478128A>G NCBI36
NG_034139.1:g.7589A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000667609.1:n.280A>G
ENST00000673647.1:c.-189+16A>G ENSP00000500967.1:n.-189+16A>G
ENST00000673996.1:n.79+1589A>G
ENST00000674069.1:c.-173+1609A>G ENSP00000501157.1:n.-173+1609A>G
ENST00000674131.1:c.-189+16A>G ENSP00000501002.1:n.-189+16A>G
ENST00000616296.4:c.-222+1589A>G ENSP00000482382.1:n.-222+1589A>G
NM_001289152.1:c.-222+1589A>G NP_001276081.1:n.-222+1589A>G
NM_001289153.1:c.-222+1609A>G NP_001276082.1:n.-222+1609A>G
NM_001289154.1:c.-173+1609A>G NP_001276083.1:n.-173+1609A>G
NM_001289152.2:c.-222+1589A>G NP_001276081.1:n.-222+1589A>G
NM_001289153.2:c.-222+1609A>G NP_001276082.1:n.-222+1609A>G
NM_001289154.2:c.-173+1609A>G NP_001276083.1:n.-173+1609A>G