Canonical Allele Identifier: CA2501340649

Gene: HOXC9 HOXC6

Linked Data

• dbSNP Id: rs2136394000
• gnomAD v3: 12-54000754-A-C
• gnomAD v4: 12-54000754-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54000754A>C , CM000674.2:g.54000754A>C	GRCh38
NC_000012.11:g.54394538A>C , CM000674.1:g.54394538A>C	GRCh37
NC_000012.10:g.52680805A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303450.5:c.538+28A>C (HOXC9) MANE Select	ENSP00000302836.4:n.538+28A>C
ENST00000303450.4:c.538+28A>C (HOXC9)	ENSP00000302836.4:n.538+28A>C
ENST00000504315.1:c.-193+9940A>C (HOXC6)	ENSP00000424124.1:n.-193+9940A>C
ENST00000504557.1:n.123-1676A>C (HOXC9)
ENST00000508190.1:c.538+28A>C (HOXC9)	ENSP00000423861.1:n.538+28A>C
ENST00000509328.1:c.-73+5738A>C (HOXC6)	ENSP00000423898.1:n.-73+5738A>C
ENST00000513209.1:c.166+14744A>C	ENSP00000476742.1:n.166+14744A>C
NM_006897.1:c.538+28A>C (HOXC9)	NP_008828.1:n.538+28A>C
NM_006897.2:c.538+28A>C (HOXC9)	NP_008828.1:n.538+28A>C
NM_006897.3:c.538+28A>C (HOXC9) MANE Select	NP_008828.1:n.538+28A>C