Canonical Allele Identifier: CA136862493

Gene: MICA

Linked Data

• dbSNP Id: rs190478978
• gnomAD v2: 6-31370001-G-T
• gnomAD v3: 6-31402224-G-T
• gnomAD v4: 6-31402224-G-T
• MyVariant Identifiers: chr6:g.31370001G>T (hg19) ; chr6:g.31402224G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402224G>T , CM000668.2:g.31402224G>T	GRCh38
NC_000006.11:g.31370001G>T , CM000668.1:g.31370001G>T	GRCh37
NC_000006.10:g.31477980G>T	NCBI36
NG_034139.1:g.7441G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.132G>T
ENST00000673647.1:c.-321G>T	ENSP00000500967.1:n.-321G>T
ENST00000673996.1:n.79+1441G>T
ENST00000674069.1:c.-173+1461G>T	ENSP00000501157.1:n.-173+1461G>T
ENST00000674131.1:c.-321G>T	ENSP00000501002.1:n.-321G>T
ENST00000616296.4:c.-222+1441G>T	ENSP00000482382.1:n.-222+1441G>T
NM_001289152.1:c.-222+1441G>T	NP_001276081.1:n.-222+1441G>T
NM_001289153.1:c.-222+1461G>T	NP_001276082.1:n.-222+1461G>T
NM_001289154.1:c.-173+1461G>T	NP_001276083.1:n.-173+1461G>T
NM_001289152.2:c.-222+1441G>T	NP_001276081.1:n.-222+1441G>T
NM_001289153.2:c.-222+1461G>T	NP_001276082.1:n.-222+1461G>T
NM_001289154.2:c.-173+1461G>T	NP_001276083.1:n.-173+1461G>T