Canonical Allele Identifier: CA136927988
Gene: C6orf10 HGNC NCBI

Linked Data

dbSNP Id: rs4713518

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32289560A>G , CM000668.2:g.32289560A>G GRCh38
NC_000006.11:g.32257337A>G , CM000668.1:g.32257337A>G GRCh37
NC_000006.10:g.32365315A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000442822.6:c.1360-891T>C ENSP00000411164.2:p.=
XM_011514236.1:c.*1487-634T>C XP_011512538.1:p.=
XM_011515039.1:c.421+26751A>G XP_011513341.1:p.=
XM_011515040.1:c.421+26751A>G XP_011513342.1:p.=
NR_136244.1:n.440+26751A>G
NR_136245.1:n.242+34146A>G
NR_136246.1:n.242+34146A>G