Canonical Allele Identifier: CA1947947971

Linked Data

dbSNP Id: rs1857064109

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1999899G>A , CM000673.2:g.1999899G>A GRCh38
NC_000011.9:g.2021129G>A , CM000673.1:g.2021129G>A GRCh37
NC_000011.8:g.1977705G>A NCBI36
NG_016165.1:g.2937C>T

Transcript Alleles

HGVS Amino-acid change
NR_131224.1:n.249+1319C>T (H19)
XM_011520273.1:c.498-11642G>A (MRPL23) XP_011518575.1:n.498-11642G>A
XM_011520274.1:c.492-11642G>A (MRPL23) XP_011518576.1:n.492-11642G>A
XM_011520275.1:c.498-11642G>A (MRPL23) XP_011518577.1:n.498-11642G>A
XM_011520275.2:c.498-11642G>A (MRPL23) XP_011518577.1:n.498-11642G>A
NM_001400176.1:c.498-11642G>A (MRPL23) NP_001387105.1:n.498-11642G>A