Canonical Allele Identifier: CA1947947976
Gene: H19 HGNC NCBI
MRPL23 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1999905C= , CM000673.2:g.1999905C= GRCh38
NC_000011.9:g.2021135C= , CM000673.1:g.2021135C= GRCh37
NC_000011.8:g.1977711C= NCBI36
NG_016165.1:g.2931G=

Transcript Alleles

HGVS Amino-acid change
NR_131224.1:n.249+1313G= (H19)
XM_011520273.1:c.498-11636C= (MRPL23) XP_011518575.1:n.498-11636C=
XM_011520274.1:c.492-11636C= (MRPL23) XP_011518576.1:n.492-11636C=
XM_011520275.1:c.498-11636C= (MRPL23) XP_011518577.1:n.498-11636C=
XM_011520275.2:c.498-11636C= (MRPL23) XP_011518577.1:n.498-11636C=
NM_001400176.1:c.498-11636C= (MRPL23) NP_001387105.1:n.498-11636C=
Search 100 bp 5'
Search 100 bp 3'