Canonical Allele Identifier: CA341969
Gene: TFAP2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.50837974G>C , CM000668.2:g.50837974G>C GRCh38
NC_000006.11:g.50805687G>C , CM000668.1:g.50805687G>C GRCh37
NC_000006.10:g.50913646G>C NCBI36
NG_008438.1:g.24249G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000393655.4:c.822-1G>C MANE Select ENSP00000377265.2:n.822-1G>C
ENST00000393655.3:c.822-1G>C ENSP00000377265.2:n.822-1G>C
NM_003221.3:c.822-1G>C NP_003212.2:n.822-1G>C
XM_006715176.2:c.822-1G>C XP_006715239.1:n.822-1G>C
XM_006715177.2:c.768-1G>C XP_006715240.1:n.768-1G>C
XM_011514834.1:c.849-1G>C XP_011513136.1:n.849-1G>C
XM_011514835.1:c.849-1G>C XP_011513137.1:n.849-1G>C
XM_011514836.1:c.849-1G>C XP_011513138.1:n.849-1G>C
XM_011514837.1:c.849-1G>C XP_011513139.1:n.849-1G>C
XM_011514837.2:c.849-1G>C XP_011513139.1:n.849-1G>C
XM_017011233.1:c.987-1G>C XP_016866722.1:n.987-1G>C
XM_017011234.1:c.951-1G>C XP_016866723.1:n.951-1G>C
XM_017011235.2:c.363-1G>C XP_016866724.1:n.363-1G>C
NM_003221.4:c.822-1G>C MANE Select NP_003212.2:n.822-1G>C
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