Canonical Allele Identifier: CA136862667

Gene: MICA

Linked Data

• dbSNP Id: rs984614633
• MyVariant Identifiers: chr6:g.31370802T>G (hg19) ; chr6:g.31403025T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31403025T>G , CM000668.2:g.31403025T>G	GRCh38
NC_000006.11:g.31370802T>G , CM000668.1:g.31370802T>G	GRCh37
NC_000006.10:g.31478781T>G	NCBI36
NG_034139.1:g.8242T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.933T>G
ENST00000673647.1:c.-188-420T>G	ENSP00000500967.1:n.-188-420T>G
ENST00000673996.1:n.79+2242T>G
ENST00000674069.1:c.-173+2262T>G	ENSP00000501157.1:n.-173+2262T>G
ENST00000674131.1:c.-188-420T>G	ENSP00000501002.1:n.-188-420T>G
ENST00000616296.4:c.-222+2242T>G	ENSP00000482382.1:n.-222+2242T>G
NM_001289152.1:c.-222+2242T>G	NP_001276081.1:n.-222+2242T>G
NM_001289153.1:c.-222+2262T>G	NP_001276082.1:n.-222+2262T>G
NM_001289154.1:c.-173+2262T>G	NP_001276083.1:n.-173+2262T>G
NM_001289152.2:c.-222+2242T>G	NP_001276081.1:n.-222+2242T>G
NM_001289153.2:c.-222+2262T>G	NP_001276082.1:n.-222+2262T>G
NM_001289154.2:c.-173+2262T>G	NP_001276083.1:n.-173+2262T>G