Canonical Allele Identifier: CA128177716
Gene: GFRA3 HGNC NCBI

Linked Data

dbSNP Id: rs762601958
gnomAD v2: 5-137599277-C-T
gnomAD v3: 5-138263588-C-T
gnomAD v4: 5-138263588-C-T
MyVariant Identifiers: chr5:g.137599277C>T (hg19) chr5:g.138263588C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138263588C>T , CM000667.2:g.138263588C>T GRCh38
NC_000005.9:g.137599277C>T , CM000667.1:g.137599277C>T GRCh37
NC_000005.8:g.137627176C>T NCBI36
NG_046894.1:g.15977G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000274721.8:c.379+673G>A MANE Select ENSP00000274721.3:n.379+673G>A
ENST00000274721.7:c.379+673G>A ENSP00000274721.3:n.379+673G>A
ENST00000378362.3:c.379+673G>A ENSP00000367613.3:n.379+673G>A
NM_001496.3:c.379+673G>A NP_001487.2:n.379+673G>A
NM_001496.4:c.379+673G>A MANE Select NP_001487.2:n.379+673G>A
Search 100 bp 5'
Search 100 bp 3'