Canonical Allele Identifier: CA2001382873
Gene: HTR3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113910159_113910160delinsGA , CM000673.2:g.113910159_113910160delinsGA GRCh38
NC_000011.9:g.113780881_113780882delinsGA , CM000673.1:g.113780881_113780882delinsGA GRCh37
NC_000011.8:g.113286091_113286092delinsGA NCBI36
NG_011483.1:g.10293_10294delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000260191.8:c.213+704_213+705delinsGA MANE Select ENSP00000260191.2:n.213+704_213+705delins...
ENST00000260191.7:c.213+704_213+705delinsGA ENSP00000260191.2:n.213+704_213+705delins...
ENST00000260191.6:c.213+704_213+705delinsGA ENSP00000260191.2:n.213+704_213+705delins...
ENST00000537778.5:c.180+704_180+705delinsGA ENSP00000443118.1:n.180+704_180+705delins...
NM_006028.4:c.213+704_213+705delinsGA NP_006019.1:n.213+704_213+705delinsGA
XM_011543063.1:c.180+704_180+705delinsGA XP_011541365.1:n.180+704_180+705delinsGA
XM_011543064.1:c.12+11076_12+11077delinsGA XP_011541366.1:n.12+11076_12+11077delinsG...
XM_011543066.1:c.180+704_180+705delinsGA XP_011541368.1:n.180+704_180+705delinsGA
NM_001363563.1:c.180+704_180+705delinsGA NP_001350492.1:n.180+704_180+705delinsGA
XM_024448767.1:c.-82+704_-82+705delinsGA XP_024304535.1:n.-82+704_-82+705delinsGA
XR_001748034.2:n.464+704_464+705delinsGA
NM_001363563.2:c.180+704_180+705delinsGA NP_001350492.1:n.180+704_180+705delinsGA
NM_006028.5:c.213+704_213+705delinsGA MANE Select NP_006019.1:n.213+704_213+705delinsGA