Canonical Allele Identifier: CA566342751

Gene: MICA

Linked Data

• dbSNP Id: rs1241994210
• gnomAD v2: 6-31370784-T-G
• gnomAD v3: 6-31403007-T-G
• gnomAD v4: 6-31403007-T-G
• MyVariant Identifiers: chr6:g.31370784T>G (hg19) ; chr6:g.31403007T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31403007T>G , CM000668.2:g.31403007T>G	GRCh38
NC_000006.11:g.31370784T>G , CM000668.1:g.31370784T>G	GRCh37
NC_000006.10:g.31478763T>G	NCBI36
NG_034139.1:g.8224T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.915T>G
ENST00000673647.1:c.-188-438T>G	ENSP00000500967.1:n.-188-438T>G
ENST00000673996.1:n.79+2224T>G
ENST00000674069.1:c.-173+2244T>G	ENSP00000501157.1:n.-173+2244T>G
ENST00000674131.1:c.-188-438T>G	ENSP00000501002.1:n.-188-438T>G
ENST00000616296.4:c.-222+2224T>G	ENSP00000482382.1:n.-222+2224T>G
NM_001289152.1:c.-222+2224T>G	NP_001276081.1:n.-222+2224T>G
NM_001289153.1:c.-222+2244T>G	NP_001276082.1:n.-222+2244T>G
NM_001289154.1:c.-173+2244T>G	NP_001276083.1:n.-173+2244T>G
NM_001289152.2:c.-222+2224T>G	NP_001276081.1:n.-222+2224T>G
NM_001289153.2:c.-222+2244T>G	NP_001276082.1:n.-222+2244T>G
NM_001289154.2:c.-173+2244T>G	NP_001276083.1:n.-173+2244T>G