Canonical Allele Identifier: CA823884287

Gene: MICA

Linked Data

• dbSNP Id: rs1282857827
• MyVariant Identifiers: chr6:g.31370334T>A (hg19) ; chr6:g.31402557T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402557T>A , CM000668.2:g.31402557T>A	GRCh38
NC_000006.11:g.31370334T>A , CM000668.1:g.31370334T>A	GRCh37
NC_000006.10:g.31478313T>A	NCBI36
NG_034139.1:g.7774T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000667609.1:n.465T>A
ENST00000673647.1:c.-189+201T>A	ENSP00000500967.1:n.-189+201T>A
ENST00000673996.1:n.79+1774T>A
ENST00000674069.1:c.-173+1794T>A	ENSP00000501157.1:n.-173+1794T>A
ENST00000674131.1:c.-189+201T>A	ENSP00000501002.1:n.-189+201T>A
ENST00000616296.4:c.-222+1774T>A	ENSP00000482382.1:n.-222+1774T>A
NM_001289152.1:c.-222+1774T>A	NP_001276081.1:n.-222+1774T>A
NM_001289153.1:c.-222+1794T>A	NP_001276082.1:n.-222+1794T>A
NM_001289154.1:c.-173+1794T>A	NP_001276083.1:n.-173+1794T>A
NM_001289152.2:c.-222+1774T>A	NP_001276081.1:n.-222+1774T>A
NM_001289153.2:c.-222+1794T>A	NP_001276082.1:n.-222+1794T>A
NM_001289154.2:c.-173+1794T>A	NP_001276083.1:n.-173+1794T>A