Canonical Allele Identifier: CA136862529

Gene: MICA

Linked Data

• dbSNP Id: rs750241059
• gnomAD v2: 6-31370215-T-C
• gnomAD v3: 6-31402438-T-C
• gnomAD v4: 6-31402438-T-C
• MyVariant Identifiers: chr6:g.31370215T>C (hg19) ; chr6:g.31402438T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402438T>C , CM000668.2:g.31402438T>C	GRCh38
NC_000006.11:g.31370215T>C , CM000668.1:g.31370215T>C	GRCh37
NC_000006.10:g.31478194T>C	NCBI36
NG_034139.1:g.7655T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.346T>C
ENST00000673647.1:c.-189+82T>C	ENSP00000500967.1:n.-189+82T>C
ENST00000673996.1:n.79+1655T>C
ENST00000674069.1:c.-173+1675T>C	ENSP00000501157.1:n.-173+1675T>C
ENST00000674131.1:c.-189+82T>C	ENSP00000501002.1:n.-189+82T>C
ENST00000616296.4:c.-222+1655T>C	ENSP00000482382.1:n.-222+1655T>C
NM_001289152.1:c.-222+1655T>C	NP_001276081.1:n.-222+1655T>C
NM_001289153.1:c.-222+1675T>C	NP_001276082.1:n.-222+1675T>C
NM_001289154.1:c.-173+1675T>C	NP_001276083.1:n.-173+1675T>C
NM_001289152.2:c.-222+1655T>C	NP_001276081.1:n.-222+1655T>C
NM_001289153.2:c.-222+1675T>C	NP_001276082.1:n.-222+1675T>C
NM_001289154.2:c.-173+1675T>C	NP_001276083.1:n.-173+1675T>C