Canonical Allele Identifier: CA10816223
Gene: METTL25B HGNC NCBI

Linked Data

dbSNP Id: rs12145743

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156730859T>G , CM000663.2:g.156730859T>G GRCh38
NC_000001.10:g.156700651T>G , CM000663.1:g.156700651T>G GRCh37
NC_000001.9:g.154967275T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368216.9:c.112-1132T>G MANE Select ENSP00000357199.4:n.112-1132T>G
ENST00000368216.8:c.112-1132T>G ENSP00000357199.4:n.112-1132T>G
ENST00000368218.8:c.112-1132T>G ENSP00000357201.4:n.112-1132T>G
ENST00000484742.5:c.-360-1132T>G ENSP00000429053.1:n.-360-1132T>G
ENST00000519086.5:c.112-1132T>G ENSP00000429756.1:n.112-1132T>G
ENST00000524343.1:c.112-1422T>G ENSP00000429389.1:n.112-1422T>G
NM_001142560.1:c.112-1132T>G NP_001136032.1:n.112-1132T>G
NM_015997.3:c.112-1132T>G NP_057081.3:n.112-1132T>G
XM_005245234.3:c.112-1132T>G XP_005245291.1:n.112-1132T>G
XM_005245235.3:c.112-1507T>G XP_005245292.1:n.112-1507T>G
XM_005245236.3:c.112-1132T>G XP_005245293.1:n.112-1132T>G
XM_005245237.3:c.112-1132T>G XP_005245294.1:n.112-1132T>G
XM_011509600.1:c.-87-1132T>G XP_011507902.1:n.-87-1132T>G
XR_426777.2:n.396-1132T>G
XR_426778.2:n.396-1132T>G
XM_005245234.5:c.112-1132T>G XP_005245291.1:n.112-1132T>G
XM_005245235.5:c.112-1507T>G XP_005245292.1:n.112-1507T>G
XM_005245236.5:c.112-1132T>G XP_005245293.1:n.112-1132T>G
XM_005245237.5:c.112-1132T>G XP_005245294.1:n.112-1132T>G
XM_017001404.1:c.-87-1132T>G XP_016856893.1:n.-87-1132T>G
XM_017001405.2:c.-479-1132T>G XP_016856894.1:n.-479-1132T>G
XM_017001406.2:c.-485-1132T>G XP_016856895.1:n.-485-1132T>G
XM_024447421.1:c.112-1132T>G XP_024303189.1:n.112-1132T>G
XR_426777.4:n.399-1132T>G
XR_426778.4:n.449-1132T>G
NM_015997.4:c.112-1132T>G MANE Select NP_057081.3:n.112-1132T>G
NM_001142560.2:c.112-1132T>G NP_001136032.1:n.112-1132T>G