Canonical Allele Identifier: CA449642880

Gene: MICA

Linked Data

• gnomAD v4: 6-31400762-T-G
• MyVariant Identifiers: chr6:g.31368539T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31400762T>G , CM000668.2:g.31400762T>G	GRCh38
NC_000006.11:g.31368539T>G , CM000668.1:g.31368539T>G	GRCh37
NC_000006.10:g.31476518T>G	NCBI36
NG_034139.1:g.5979T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000667609.1:n.63T>G
ENST00000673647.1:c.-390T>G	ENSP00000500967.1:n.-390T>G
ENST00000673996.1:n.58T>G
ENST00000674069.1:c.-174T>G	ENSP00000501157.1:n.-174T>G
ENST00000674131.1:c.-410T>G	ENSP00000501002.1:n.-410T>G
ENST00000616296.4:c.-243T>G	ENSP00000482382.1:n.-243T>G
NM_001289152.1:c.-243T>G	NP_001276081.1:n.-243T>G
NM_001289153.1:c.-223T>G	NP_001276082.1:n.-223T>G
NM_001289154.1:c.-174T>G	NP_001276083.1:n.-174T>G
NM_001289152.2:c.-243T>G	NP_001276081.1:n.-243T>G
NM_001289153.2:c.-223T>G	NP_001276082.1:n.-223T>G
NM_001289154.2:c.-174T>G	NP_001276083.1:n.-174T>G