Canonical Allele Identifier: CA74792079

Gene: DOCK3

Linked Data

• dbSNP Id: rs13088462
• gnomAD v2: 3-51071713-T-C
• gnomAD v3: 3-51034282-T-C
• gnomAD v4: 3-51034282-T-C
• MyVariant Identifiers: chr3:g.51071713T>C (hg19) ; chr3:g.51034282T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.51034282T>C , CM000665.2:g.51034282T>C	GRCh38
NC_000003.11:g.51071713T>C , CM000665.1:g.51071713T>C	GRCh37
NC_000003.10:g.51046753T>C	NCBI36
NG_028012.1:g.364042T>C
NG_028012.2:g.364042T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000266037.10:c.316-30166T>C MANE Select	ENSP00000266037.8:n.316-30166T>C
ENST00000266037.9:c.316-30166T>C	ENSP00000266037.8:n.316-30166T>C
NM_004947.4:c.316-30166T>C	NP_004938.1:n.316-30166T>C
XM_005264914.2:c.316-30166T>C	XP_005264971.1:n.316-30166T>C
XM_005264915.2:c.316-30166T>C	XP_005264972.1:n.316-30166T>C
XM_005264916.2:c.316-30166T>C	XP_005264973.1:n.316-30166T>C
XM_005264917.2:c.316-30166T>C	XP_005264974.1:n.316-30166T>C
XM_005264918.2:c.316-30166T>C	XP_005264975.1:n.316-30166T>C
XM_006713008.2:c.316-30166T>C	XP_006713071.1:n.316-30166T>C
XM_006713009.2:c.316-30166T>C	XP_006713072.1:n.316-30166T>C
XM_006713010.2:c.316-30166T>C	XP_006713073.1:n.316-30166T>C
XM_011533446.1:c.316-30166T>C	XP_011531748.1:n.316-30166T>C
XM_005264914.3:c.316-30166T>C	XP_005264971.1:n.316-30166T>C
XM_005264915.3:c.316-30166T>C	XP_005264972.1:n.316-30166T>C
XM_005264916.4:c.316-30166T>C	XP_005264973.1:n.316-30166T>C
XM_005264917.3:c.316-30166T>C	XP_005264974.1:n.316-30166T>C
XM_005264918.4:c.316-30166T>C	XP_005264975.1:n.316-30166T>C
XM_006713008.3:c.316-30166T>C	XP_006713071.1:n.316-30166T>C
XM_006713009.3:c.316-30166T>C	XP_006713072.1:n.316-30166T>C
XM_006713010.3:c.316-30166T>C	XP_006713073.1:n.316-30166T>C
XM_017005825.2:c.316-30166T>C	XP_016861314.1:n.316-30166T>C
XM_017005826.2:c.316-30166T>C	XP_016861315.1:n.316-30166T>C
NM_004947.5:c.316-30166T>C MANE Select	NP_004938.1:n.316-30166T>C