Canonical Allele Identifier: CA499649638

Gene: STAC2

Linked Data

• MyVariant Identifiers: chr17:g.37374169A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39217916A>G , CM000679.2:g.39217916A>G	GRCh38
NC_000017.10:g.37374169A>G , CM000679.1:g.37374169A>G	GRCh37
NC_000017.9:g.34627695A>G	NCBI36
NG_054936.1:g.12872T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333461.6:c.348T>C MANE Select	ENSP00000327509.5:p.His116=
ENST00000333461.5:c.348T>C	ENSP00000327509.5:p.His116=
ENST00000584501.1:c.195+153T>C	ENSP00000463299.1:n.195+153T>C
NM_198993.3:c.348T>C	NP_945344.1:p.His116=
NM_001351360.1:c.-30+153T>C	NP_001338289.1:n.-30+153T>C
NM_198993.4:c.348T>C	NP_945344.1:p.His116=
XM_017024580.1:c.348T>C	XP_016880069.1:p.His116=
XM_017024581.1:c.348T>C	XP_016880070.1:p.His116=
XM_017024583.1:c.348T>C	XP_016880072.1:p.His116=
XR_002957997.1:n.633T>C
NM_198993.5:c.348T>C MANE Select	NP_945344.1:p.His116=
NM_001351360.2:c.-30+153T>C	NP_001338289.1:n.-30+153T>C