Canonical Allele Identifier: CA1538250018
Gene: C1QTNF3-AMACR HGNC NCBI

Linked Data

dbSNP Id: rs1754066272

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34008174A>C , CM000667.2:g.34008174A>C GRCh38
NC_000005.9:g.34008279A>C , CM000667.1:g.34008279A>C GRCh37
NC_000005.8:g.34044036A>C NCBI36
NG_016211.1:g.4942T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382079.3:c.690-2275T>G ENSP00000371511.3:n.690-2275T>G
NR_037951.1:n.765-2275T>G