Canonical Allele Identifier: CA136862518

Gene: MICA

Linked Data

• dbSNP Id: rs9266800
• gnomAD v2: 6-31370147-A-C
• gnomAD v3: 6-31402370-A-C
• gnomAD v4: 6-31402370-A-C
• MyVariant Identifiers: chr6:g.31370147A>C (hg19) ; chr6:g.31402370A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402370A>C , CM000668.2:g.31402370A>C	GRCh38
NC_000006.11:g.31370147A>C , CM000668.1:g.31370147A>C	GRCh37
NC_000006.10:g.31478126A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.278A>C
ENST00000673647.1:c.-189+14A>C	ENSP00000500967.1:n.-189+14A>C
ENST00000673996.1:n.79+1587A>C
ENST00000674069.1:c.-173+1607A>C	ENSP00000501157.1:n.-173+1607A>C
ENST00000674131.1:c.-189+14A>C	ENSP00000501002.1:n.-189+14A>C
ENST00000616296.4:c.-222+1587A>C	ENSP00000482382.1:n.-222+1587A>C
NM_001289152.1:c.-222+1587A>C	NP_001276081.1:n.-222+1587A>C
NM_001289153.1:c.-222+1607A>C	NP_001276082.1:n.-222+1607A>C
NM_001289154.1:c.-173+1607A>C	NP_001276083.1:n.-173+1607A>C
NM_001289152.2:c.-222+1587A>C	NP_001276081.1:n.-222+1587A>C
NM_001289153.2:c.-222+1607A>C	NP_001276082.1:n.-222+1607A>C
NM_001289154.2:c.-173+1607A>C	NP_001276083.1:n.-173+1607A>C