Canonical Allele Identifier: CA347179590
Gene: CD207 HGNC NCBI

Linked Data

gnomAD v4: 2-70831807-T-C
MyVariant Identifiers: chr2:g.71058938T>C (hg19) chr2:g.70831807T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831807T>C , CM000664.2:g.70831807T>C GRCh38
NC_000002.11:g.71058938T>C , CM000664.1:g.71058938T>C GRCh37
NC_000002.10:g.70912446T>C NCBI36
NG_033914.1:g.9017A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.730A>G MANE Select ENSP00000386378.3:p.Lys244Glu
ENST00000410009.4:c.730A>G ENSP00000386378.3:p.Lys244Glu
NM_015717.4:c.730A>G NP_056532.4:p.Lys244Glu
XM_011532874.1:c.730A>G XP_011531176.1:p.Lys244Glu
XM_011532875.1:c.730A>G XP_011531177.1:p.Lys244Glu
XM_011532876.1:c.730A>G XP_011531178.1:p.Lys244Glu
XM_011532875.2:c.730A>G XP_011531177.1:p.Lys244Glu
XM_011532876.2:c.730A>G XP_011531178.1:p.Lys244Glu
NM_015717.5:c.730A>G MANE Select NP_056532.4:p.Lys244Glu
Search 100 bp 5'
Search 100 bp 3'