Canonical Allele Identifier: CA449643791

Gene: MICA

Linked Data

• gnomAD v4: 6-31402242-A-G
• MyVariant Identifiers: chr6:g.31370019A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402242A>G , CM000668.2:g.31402242A>G	GRCh38
NC_000006.11:g.31370019A>G , CM000668.1:g.31370019A>G	GRCh37
NC_000006.10:g.31477998A>G	NCBI36
NG_034139.1:g.7459A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.150A>G
ENST00000673647.1:c.-303A>G	ENSP00000500967.1:n.-303A>G
ENST00000673996.1:n.79+1459A>G
ENST00000674069.1:c.-173+1479A>G	ENSP00000501157.1:n.-173+1479A>G
ENST00000674131.1:c.-303A>G	ENSP00000501002.1:n.-303A>G
ENST00000616296.4:c.-222+1459A>G	ENSP00000482382.1:n.-222+1459A>G
NM_001289152.1:c.-222+1459A>G	NP_001276081.1:n.-222+1459A>G
NM_001289153.1:c.-222+1479A>G	NP_001276082.1:n.-222+1479A>G
NM_001289154.1:c.-173+1479A>G	NP_001276083.1:n.-173+1479A>G
NM_001289152.2:c.-222+1459A>G	NP_001276081.1:n.-222+1459A>G
NM_001289153.2:c.-222+1479A>G	NP_001276082.1:n.-222+1479A>G
NM_001289154.2:c.-173+1479A>G	NP_001276083.1:n.-173+1479A>G