Canonical Allele Identifier: CA347179521

Gene: CD207

Linked Data

• dbSNP Id: rs2104700277
• MyVariant Identifiers: chr2:g.71058907C>G (hg19) ; chr2:g.70831776C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831776C>G , CM000664.2:g.70831776C>G	GRCh38
NC_000002.11:g.71058907C>G , CM000664.1:g.71058907C>G	GRCh37
NC_000002.10:g.70912415C>G	NCBI36
NG_033914.1:g.9048G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.761G>C MANE Select	ENSP00000386378.3:p.Gly254Ala
ENST00000410009.4:c.761G>C	ENSP00000386378.3:p.Gly254Ala
NM_015717.4:c.761G>C	NP_056532.4:p.Gly254Ala
XM_011532874.1:c.761G>C	XP_011531176.1:p.Gly254Ala
XM_011532875.1:c.761G>C	XP_011531177.1:p.Gly254Ala
XM_011532876.1:c.761G>C	XP_011531178.1:p.Gly254Ala
XM_011532875.2:c.761G>C	XP_011531177.1:p.Gly254Ala
XM_011532876.2:c.761G>C	XP_011531178.1:p.Gly254Ala
NM_015717.5:c.761G>C MANE Select	NP_056532.4:p.Gly254Ala