Canonical Allele Identifier: CA501202299

Gene: SMARCD2

Linked Data

• gnomAD v4: 17-63837470-C-A
• MyVariant Identifiers: chr17:g.61914830C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837470C>A , CM000679.2:g.63837470C>A	GRCh38
NC_000017.10:g.61914830C>A , CM000679.1:g.61914830C>A	GRCh37
NC_000017.9:g.59268562C>A	NCBI36
NG_053004.1:g.10522G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.260G>T
ENST00000698015.1:n.6G>T
ENST00000698016.1:c.231G>T	ENSP00000513502.1:p.Ala77=
ENST00000698021.1:c.35G>T
ENST00000698022.1:c.189G>T	ENSP00000513504.1:p.Ala63=
ENST00000698027.1:c.231G>T	ENSP00000513505.1:p.Ala77=
ENST00000448276.7:c.372G>T MANE Select	ENSP00000392617.2:p.Ala124=
ENST00000225742.13:c.147G>T	ENSP00000225742.9:p.Ala49=
ENST00000323347.14:c.228G>T	ENSP00000318451.10:p.Ala76=
ENST00000448276.6:c.372G>T	ENSP00000392617.2:p.Ala124=
ENST00000577686.1:n.53-233G>T
ENST00000580054.1:c.156G>T	ENSP00000463793.1:p.Ala52=
ENST00000584400.5:c.217-233G>T	ENSP00000464503.1:n.217-233G>T
ENST00000613943.4:c.261G>T	ENSP00000483605.1:p.Ala87=
NM_001098426.1:c.372G>T	NP_001091896.1:p.Ala124=
XM_005257604.2:c.147G>T	XP_005257661.2:p.Ala49=
NM_001330439.1:c.147G>T	NP_001317368.1:p.Ala49=
NM_001330440.1:c.228G>T	NP_001317369.1:p.Ala76=
NM_001098426.2:c.372G>T MANE Select	NP_001091896.1:p.Ala124=
NM_001330440.2:c.228G>T	NP_001317369.1:p.Ala76=