Canonical Allele Identifier: CA490314055

Gene: HDC

Linked Data

• dbSNP Id: rs1595697679
• MyVariant Identifiers: chr15:g.50534637A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242440A>G , CM000677.2:g.50242440A>G	GRCh38
NC_000015.9:g.50534637A>G , CM000677.1:g.50534637A>G	GRCh37
NC_000015.8:g.48321929A>G	NCBI36
NG_027487.1:g.28526T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1809T>C MANE Select	ENSP00000267845.3:p.Ser603=
ENST00000267845.7:c.1809T>C	ENSP00000267845.3:p.Ser603=
ENST00000543581.5:c.1710T>C	ENSP00000440252.1:p.Ser570=
ENST00000559816.1:n.1553T>C
NM_001306146.1:c.1710T>C	NP_001293075.1:p.Ser570=
NM_002112.3:c.1809T>C	NP_002103.2:p.Ser603=
XM_011521479.1:c.1572T>C	XP_011519781.1:p.Ser524=
XM_011521480.1:c.1377T>C	XP_011519782.1:p.Ser459=
XM_017022094.1:c.1914T>C	XP_016877583.1:p.Ser638=
XM_017022095.1:c.1815T>C	XP_016877584.1:p.Ser605=
XM_017022096.1:c.1686T>C	XP_016877585.1:p.Ser562=
XM_017022097.1:c.1677T>C	XP_016877586.1:p.Ser559=
XM_017022098.1:c.1482T>C	XP_016877587.1:p.Ser494=
NM_002112.4:c.1809T>C MANE Select	NP_002103.2:p.Ser603=
NM_001306146.2:c.1710T>C	NP_001293075.1:p.Ser570=