Canonical Allele Identifier: CA347179343

Gene: CD207

Linked Data

• MyVariant Identifiers: chr2:g.71058830A>G (hg19) ; chr2:g.70831699A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831699A>G , CM000664.2:g.70831699A>G	GRCh38
NC_000002.11:g.71058830A>G , CM000664.1:g.71058830A>G	GRCh37
NC_000002.10:g.70912338A>G	NCBI36
NG_033914.1:g.9125T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.836+2T>C MANE Select	ENSP00000386378.3:n.836+2T>C
ENST00000410009.4:c.836+2T>C	ENSP00000386378.3:n.836+2T>C
NM_015717.4:c.836+2T>C	NP_056532.4:n.836+2T>C
XM_011532874.1:c.836+2T>C	XP_011531176.1:n.836+2T>C
XM_011532875.1:c.836+2T>C	XP_011531177.1:n.836+2T>C
XM_011532876.1:c.836+2T>C	XP_011531178.1:n.836+2T>C
XM_011532875.2:c.836+2T>C	XP_011531177.1:n.836+2T>C
XM_011532876.2:c.836+2T>C	XP_011531178.1:n.836+2T>C
NM_015717.5:c.836+2T>C MANE Select	NP_056532.4:n.836+2T>C