Canonical Allele Identifier: CA364410064

Gene: TFAP2B

Linked Data

• MyVariant Identifiers: chr6:g.50786660A>C (hg19) ; chr6:g.50818947A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50818947A>C , CM000668.2:g.50818947A>C	GRCh38
NC_000006.11:g.50786660A>C , CM000668.1:g.50786660A>C	GRCh37
NC_000006.10:g.50894619A>C	NCBI36
NG_008438.1:g.5222A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000393655.4:c.56A>C MANE Select	ENSP00000377265.2:p.Asn19Thr
ENST00000344788.7:c.23A>C	ENSP00000342252.3:p.Asn8Thr
ENST00000393655.3:c.56A>C	ENSP00000377265.2:p.Asn19Thr
NM_003221.3:c.56A>C	NP_003212.2:p.Asn19Thr
XM_006715176.2:c.56A>C	XP_006715239.1:p.Asn19Thr
XM_011514834.1:c.56A>C	XP_011513136.1:p.Asn19Thr
XM_011514835.1:c.56A>C	XP_011513137.1:p.Asn19Thr
XM_011514836.1:c.56A>C	XP_011513138.1:p.Asn19Thr
XM_011514837.1:c.56A>C	XP_011513139.1:p.Asn19Thr
XM_011514837.2:c.56A>C	XP_011513139.1:p.Asn19Thr
XM_017011233.1:c.148A>C	XP_016866722.1:p.Met50Leu
XM_017011234.1:c.112A>C	XP_016866723.1:p.Met38Leu
XM_017011235.2:c.56A>C	XP_016866724.1:p.Asn19Thr
NM_003221.4:c.56A>C MANE Select	NP_003212.2:p.Asn19Thr