Canonical Allele Identifier: CA136862647

Gene: MICA

Linked Data

• dbSNP Id: rs536364279
• gnomAD v2: 6-31370736-G-A
• gnomAD v3: 6-31402959-G-A
• gnomAD v4: 6-31402959-G-A
• MyVariant Identifiers: chr6:g.31370736G>A (hg19) ; chr6:g.31402959G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402959G>A , CM000668.2:g.31402959G>A	GRCh38
NC_000006.11:g.31370736G>A , CM000668.1:g.31370736G>A	GRCh37
NC_000006.10:g.31478715G>A	NCBI36
NG_034139.1:g.8176G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.867G>A
ENST00000673647.1:c.-188-486G>A	ENSP00000500967.1:n.-188-486G>A
ENST00000673996.1:n.79+2176G>A
ENST00000674069.1:c.-173+2196G>A	ENSP00000501157.1:n.-173+2196G>A
ENST00000674131.1:c.-188-486G>A	ENSP00000501002.1:n.-188-486G>A
ENST00000616296.4:c.-222+2176G>A	ENSP00000482382.1:n.-222+2176G>A
NM_001289152.1:c.-222+2176G>A	NP_001276081.1:n.-222+2176G>A
NM_001289153.1:c.-222+2196G>A	NP_001276082.1:n.-222+2196G>A
NM_001289154.1:c.-173+2196G>A	NP_001276083.1:n.-173+2196G>A
NM_001289152.2:c.-222+2176G>A	NP_001276081.1:n.-222+2176G>A
NM_001289153.2:c.-222+2196G>A	NP_001276082.1:n.-222+2196G>A
NM_001289154.2:c.-173+2196G>A	NP_001276083.1:n.-173+2196G>A