Canonical Allele Identifier: CA2690634861
Gene: ROR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91950120G>A , CM000671.2:g.91950120G>A GRCh38
NC_000009.11:g.94712402G>A , CM000671.1:g.94712402G>A GRCh37
NC_000009.10:g.93752223G>A NCBI36
NG_008089.1:g.5043C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.-157C>T MANE Select ENSP00000364860.3:n.-157C>T
ENST00000375708.3:c.-157C>T ENSP00000364860.3:n.-157C>T
NM_004560.3:c.-157C>T NP_004551.2:n.-157C>T
NM_001318204.1:c.-157C>T NP_001305133.1:n.-157C>T
XR_001746315.1:n.87C>T
NM_004560.4:c.-157C>T MANE Select NP_004551.2:n.-157C>T
NM_001318204.2:c.-157C>T NP_001305133.1:n.-157C>T