Canonical Allele Identifier: CA566342741

Gene: MICA

Linked Data

• dbSNP Id: rs1238799666
• gnomAD v2: 6-31370446-T-A
• gnomAD v3: 6-31402669-T-A
• gnomAD v4: 6-31402669-T-A
• MyVariant Identifiers: chr6:g.31370446T>A (hg19) ; chr6:g.31402669T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402669T>A , CM000668.2:g.31402669T>A	GRCh38
NC_000006.11:g.31370446T>A , CM000668.1:g.31370446T>A	GRCh37
NC_000006.10:g.31478425T>A	NCBI36
NG_034139.1:g.7886T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.577T>A
ENST00000673647.1:c.-189+313T>A	ENSP00000500967.1:n.-189+313T>A
ENST00000673996.1:n.79+1886T>A
ENST00000674069.1:c.-173+1906T>A	ENSP00000501157.1:n.-173+1906T>A
ENST00000674131.1:c.-189+313T>A	ENSP00000501002.1:n.-189+313T>A
ENST00000616296.4:c.-222+1886T>A	ENSP00000482382.1:n.-222+1886T>A
NM_001289152.1:c.-222+1886T>A	NP_001276081.1:n.-222+1886T>A
NM_001289153.1:c.-222+1906T>A	NP_001276082.1:n.-222+1906T>A
NM_001289154.1:c.-173+1906T>A	NP_001276083.1:n.-173+1906T>A
NM_001289152.2:c.-222+1886T>A	NP_001276081.1:n.-222+1886T>A
NM_001289153.2:c.-222+1906T>A	NP_001276082.1:n.-222+1906T>A
NM_001289154.2:c.-173+1906T>A	NP_001276083.1:n.-173+1906T>A