Canonical Allele Identifier: CA449642874

Gene: MICA

Linked Data

• gnomAD v4: 6-31400761-C-T
• MyVariant Identifiers: chr6:g.31368538C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31400761C>T , CM000668.2:g.31400761C>T	GRCh38
NC_000006.11:g.31368538C>T , CM000668.1:g.31368538C>T	GRCh37
NC_000006.10:g.31476517C>T	NCBI36
NG_034139.1:g.5978C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.62C>T
ENST00000673647.1:c.-391C>T	ENSP00000500967.1:n.-391C>T
ENST00000673996.1:n.57C>T
ENST00000674069.1:c.-175C>T	ENSP00000501157.1:n.-175C>T
ENST00000674131.1:c.-411C>T	ENSP00000501002.1:n.-411C>T
ENST00000616296.4:c.-244C>T	ENSP00000482382.1:n.-244C>T
NM_001289152.1:c.-244C>T	NP_001276081.1:n.-244C>T
NM_001289153.1:c.-224C>T	NP_001276082.1:n.-224C>T
NM_001289154.1:c.-175C>T	NP_001276083.1:n.-175C>T
NM_001289152.2:c.-244C>T	NP_001276081.1:n.-244C>T
NM_001289153.2:c.-224C>T	NP_001276082.1:n.-224C>T
NM_001289154.2:c.-175C>T	NP_001276083.1:n.-175C>T