Canonical Allele Identifier: CA136862581

Gene: MICA

Linked Data

• dbSNP Id: rs536325750
• gnomAD v3: 6-31402550-A-T
• gnomAD v4: 6-31402550-A-T
• MyVariant Identifiers: chr6:g.31370327A>T (hg19) ; chr6:g.31402550A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402550A>T , CM000668.2:g.31402550A>T	GRCh38
NC_000006.11:g.31370327A>T , CM000668.1:g.31370327A>T	GRCh37
NC_000006.10:g.31478306A>T	NCBI36
NG_034139.1:g.7767A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000667609.1:n.458A>T
ENST00000673647.1:c.-189+194A>T	ENSP00000500967.1:n.-189+194A>T
ENST00000673996.1:n.79+1767A>T
ENST00000674069.1:c.-173+1787A>T	ENSP00000501157.1:n.-173+1787A>T
ENST00000674131.1:c.-189+194A>T	ENSP00000501002.1:n.-189+194A>T
ENST00000616296.4:c.-222+1767A>T	ENSP00000482382.1:n.-222+1767A>T
NM_001289152.1:c.-222+1767A>T	NP_001276081.1:n.-222+1767A>T
NM_001289153.1:c.-222+1787A>T	NP_001276082.1:n.-222+1787A>T
NM_001289154.1:c.-173+1787A>T	NP_001276083.1:n.-173+1787A>T
NM_001289152.2:c.-222+1767A>T	NP_001276081.1:n.-222+1767A>T
NM_001289153.2:c.-222+1787A>T	NP_001276082.1:n.-222+1787A>T
NM_001289154.2:c.-173+1787A>T	NP_001276083.1:n.-173+1787A>T