Canonical Allele Identifier: CA10793878

Gene: GPR137B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236146724A>C , CM000663.2:g.236146724A>C	GRCh38
NC_000001.10:g.236310024A>C , CM000663.1:g.236310024A>C	GRCh37
NC_000001.9:g.234376647A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366592.8:c.414+3688A>C MANE Select	ENSP00000355551.3:n.414+3688A>C
ENST00000366591.4:n.493+3688A>C
ENST00000366592.7:c.414+3688A>C	ENSP00000355551.3:n.414+3688A>C
ENST00000419162.5:c.414+3688A>C	ENSP00000401841.2:n.414+3688A>C
NM_003272.3:c.414+3688A>C	NP_003263.1:n.414+3688A>C
XR_247039.2:n.535+3688A>C
XM_017002209.2:c.414+3688A>C	XP_016857698.1:n.414+3688A>C
XM_017002210.2:c.414+3688A>C	XP_016857699.1:n.414+3688A>C
XR_247039.4:n.508+3688A>C
NM_003272.4:c.414+3688A>C MANE Select	NP_003263.1:n.414+3688A>C