Canonical Allele Identifier: CA39657255
Gene: GPR137B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236149827T>C , CM000663.2:g.236149827T>C GRCh38
NC_000001.10:g.236313127T>C , CM000663.1:g.236313127T>C GRCh37
NC_000001.9:g.234379750T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366592.8:c.414+6791T>C MANE Select ENSP00000355551.3:n.414+6791T>C
ENST00000366591.4:n.493+6791T>C
ENST00000366592.7:c.414+6791T>C ENSP00000355551.3:n.414+6791T>C
ENST00000419162.5:c.414+6791T>C ENSP00000401841.2:n.414+6791T>C
NM_003272.3:c.414+6791T>C NP_003263.1:n.414+6791T>C
XR_247039.2:n.535+6791T>C
XM_017002209.2:c.414+6791T>C XP_016857698.1:n.414+6791T>C
XM_017002210.2:c.414+6791T>C XP_016857699.1:n.414+6791T>C
XR_247039.4:n.508+6791T>C
NM_003272.4:c.414+6791T>C MANE Select NP_003263.1:n.414+6791T>C
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