Canonical Allele Identifier: CA1619181829

Gene: MICB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31499588C= , CM000668.2:g.31499588C=	GRCh38
NC_000006.11:g.31467365C= , CM000668.1:g.31467365C=	GRCh37
NC_000006.10:g.31575344C=	NCBI36
NG_021405.1:g.6511C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005931.5:c.70+1325C= MANE Select	NP_005922.2:n.70+1325C=
ENST00000252229.7:c.70+1325C= MANE Select	ENSP00000252229.6:n.70+1325C=
NM_001289160.1:c.-27+4593C=	NP_001276089.1:n.-27+4593C=
NM_001289160.2:c.-27+4593C=	NP_001276089.1:n.-27+4593C=
NM_001289161.1:c.70+1325C=	NP_001276090.1:n.70+1325C=
NM_001289161.2:c.70+1325C=	NP_001276090.1:n.70+1325C=
NM_005931.4:c.70+1325C=	NP_005922.2:n.70+1325C=
ENST00000252229.6:c.70+1325C=	ENSP00000252229.6:n.70+1325C=
ENST00000399150.7:c.70+1325C=	ENSP00000382103.3:n.70+1325C=
ENST00000538442.5:c.-27+4593C=	ENSP00000442345.1:n.-27+4593C=
XM_011514630.1:c.-27+4612C=	XP_011512932.1:n.-27+4612C=
XM_011514631.1:c.-27+2688C=	XP_011512933.1:n.-27+2688C=