Canonical Allele Identifier: CA449642841

Gene: MICA

Linked Data

• gnomAD v4: 6-31400755-T-A
• MyVariant Identifiers: chr6:g.31368532T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31400755T>A , CM000668.2:g.31400755T>A	GRCh38
NC_000006.11:g.31368532T>A , CM000668.1:g.31368532T>A	GRCh37
NC_000006.10:g.31476511T>A	NCBI36
NG_034139.1:g.5972T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.56T>A
ENST00000673647.1:c.-397T>A	ENSP00000500967.1:n.-397T>A
ENST00000673996.1:n.51T>A
ENST00000674069.1:c.-181T>A	ENSP00000501157.1:n.-181T>A
ENST00000674131.1:c.-417T>A	ENSP00000501002.1:n.-417T>A
ENST00000616296.4:c.-250T>A	ENSP00000482382.1:n.-250T>A
NM_001289152.1:c.-250T>A	NP_001276081.1:n.-250T>A
NM_001289153.1:c.-230T>A	NP_001276082.1:n.-230T>A
NM_001289154.1:c.-181T>A	NP_001276083.1:n.-181T>A
NM_001289152.2:c.-250T>A	NP_001276081.1:n.-250T>A
NM_001289153.2:c.-230T>A	NP_001276082.1:n.-230T>A
NM_001289154.2:c.-181T>A	NP_001276083.1:n.-181T>A