Canonical Allele Identifier: CA1585788199
Gene: GFRA3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138263567A= , CM000667.2:g.138263567A= GRCh38
NC_000005.9:g.137599256A= , CM000667.1:g.137599256A= GRCh37
NC_000005.8:g.137627155A= NCBI36
NG_046894.1:g.15998T=

Transcript Alleles

HGVS Amino-acid change
ENST00000274721.8:c.379+694T= MANE Select ENSP00000274721.3:n.379+694T=
ENST00000274721.7:c.379+694T= ENSP00000274721.3:n.379+694T=
ENST00000378362.3:c.379+694T= ENSP00000367613.3:n.379+694T=
NM_001496.3:c.379+694T= NP_001487.2:n.379+694T=
NM_001496.4:c.379+694T= MANE Select NP_001487.2:n.379+694T=
Search 100 bp 5'
Search 100 bp 3'