Canonical Allele Identifier: CA823903898

Gene: MICB

Linked Data

• dbSNP Id: rs3132464
• gnomAD v4: 6-31509684-C-G
• MyVariant Identifiers: chr6:g.31477461C>G (hg19) ; chr6:g.31509684C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31509684C>G , CM000668.2:g.31509684C>G	GRCh38
NC_000006.11:g.31477461C>G , CM000668.1:g.31477461C>G	GRCh37
NC_000006.10:g.31585440C>G	NCBI36
NG_021405.1:g.16607C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252229.7:c.1025-98C>G MANE Select	ENSP00000252229.6:n.1025-98C>G
ENST00000252229.6:c.1025-98C>G	ENSP00000252229.6:n.1025-98C>G
ENST00000399150.7:c.896-98C>G	ENSP00000382103.3:n.896-98C>G
ENST00000538442.5:c.929-98C>G	ENSP00000442345.1:n.929-98C>G
NM_001289160.1:c.929-98C>G	NP_001276089.1:n.929-98C>G
NM_001289161.1:c.896-98C>G	NP_001276090.1:n.896-98C>G
NM_005931.4:c.1025-98C>G	NP_005922.2:n.1025-98C>G
XM_011514630.1:c.929-98C>G	XP_011512932.1:n.929-98C>G
XM_011514631.1:c.929-98C>G	XP_011512933.1:n.929-98C>G
NM_005931.5:c.1025-98C>G MANE Select	NP_005922.2:n.1025-98C>G
NM_001289161.2:c.896-98C>G	NP_001276090.1:n.896-98C>G
NM_001289160.2:c.929-98C>G	NP_001276089.1:n.929-98C>G