Canonical Allele Identifier: CA3658773

Gene: GMNN

Linked Data

• ClinVar Variation Id: 3049761
• ClinVar RCV Id: RCV003961497
• dbSNP Id: rs148482261
• ExAC: 6:24777466 A / G
• gnomAD v2: 6-24777466-A-G
• gnomAD v3: 6-24777238-A-G
• gnomAD v4: 6-24777238-A-G
• MyVariant Identifiers: chr6:g.24777466A>G (hg19) ; chr6:g.24777238A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24777238A>G , CM000668.2:g.24777238A>G	GRCh38
NC_000006.11:g.24777466A>G , CM000668.1:g.24777466A>G	GRCh37
NC_000006.10:g.24885445A>G	NCBI36
NG_030440.1:g.7308A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230056.8:c.-9A>G MANE Select	ENSP00000230056.3:n.-9A>G
ENST00000230056.7:c.-9A>G	ENSP00000230056.3:n.-9A>G
ENST00000356509.7:c.-9A>G	ENSP00000348902.3:n.-9A>G
ENST00000378054.6:c.-9A>G	ENSP00000367293.2:n.-9A>G
ENST00000378059.3:c.-9A>G	ENSP00000367298.3:n.-9A>G
ENST00000468943.1:n.181A>G
ENST00000476555.5:c.-9A>G	ENSP00000419584.1:n.-9A>G
ENST00000620958.4:c.-9A>G	ENSP00000477506.1:n.-9A>G
NM_001251989.1:c.-9A>G	NP_001238918.1:n.-9A>G
NM_001251990.1:c.-9A>G	NP_001238919.1:n.-9A>G
NM_001251991.1:c.-9A>G	NP_001238920.1:n.-9A>G
NM_015895.4:c.-9A>G	NP_056979.1:n.-9A>G
XM_005249159.1:c.-9A>G	XP_005249216.1:n.-9A>G
XM_005249159.2:c.-9A>G	XP_005249216.1:n.-9A>G
NM_015895.5:c.-9A>G MANE Select	NP_056979.1:n.-9A>G
NM_001251989.2:c.-9A>G	NP_001238918.1:n.-9A>G
NM_001251990.2:c.-9A>G	NP_001238919.1:n.-9A>G