Canonical Allele Identifier: CA2831214428
Gene: CD207 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831991G>C , CM000664.2:g.70831991G>C GRCh38
NC_000002.11:g.71059122G>C , CM000664.1:g.71059122G>C GRCh37
NC_000002.10:g.70912630G>C NCBI36
NG_033914.1:g.8833C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.718-172C>G MANE Select ENSP00000386378.3:n.718-172C>G
ENST00000410009.4:c.718-172C>G ENSP00000386378.3:n.718-172C>G
NM_015717.4:c.718-172C>G NP_056532.4:n.718-172C>G
XM_011532874.1:c.718-172C>G XP_011531176.1:n.718-172C>G
XM_011532875.1:c.718-172C>G XP_011531177.1:n.718-172C>G
XM_011532876.1:c.718-172C>G XP_011531178.1:n.718-172C>G
XM_011532875.2:c.718-172C>G XP_011531177.1:n.718-172C>G
XM_011532876.2:c.718-172C>G XP_011531178.1:n.718-172C>G
NM_015717.5:c.718-172C>G MANE Select NP_056532.4:n.718-172C>G
Search 100 bp 5'
Search 100 bp 3'