Canonical Allele Identifier: CA3497876
Gene: HTR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148476770G>A , CM000667.2:g.148476770G>A GRCh38
NC_000005.9:g.147856333G>A , CM000667.1:g.147856333G>A GRCh37
NC_000005.8:g.147836526G>A NCBI36
NG_029052.1:g.182407C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001040169.2:c.1077-25498C>T NP_001035259.1:n.1077-25498C>T
NM_001040172.2:c.1077-25C>T NP_001035262.2:n.1077-25C>T
NM_199453.3:c.1077-10845C>T NP_955525.1:n.1077-10845C>T
ENST00000517929.5:c.1077-25C>T ENSP00000435904.1:n.1077-25C>T
ENST00000521530.5:c.1077-25498C>T ENSP00000428320.1:n.1077-25498C>T
ENST00000521530.6:c.1077-25498C>T ENSP00000428320.1:n.1077-25498C>T
ENST00000521735.5:c.1077-10845C>T ENSP00000430979.1:n.1077-10845C>T
ENST00000522588.5:c.1077-10845C>T ENSP00000430874.1:n.1077-10845C>T
XR_001742935.1:n.776+7753G>A