Canonical Allele Identifier: CA304392203

Gene: MATK

Linked Data

• dbSNP Id: rs910093980
• MyVariant Identifiers: chr19:g.3797078G>A (hg19) ; chr19:g.3797080G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3797080G>A , CM000681.2:g.3797080G>A	GRCh38
NC_000019.9:g.3797078G>A , CM000681.1:g.3797078G>A	GRCh37
NC_000019.8:g.3748078G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000395045.6:c.-58+4452C>T	ENSP00000378485.1:n.-58+4452C>T
ENST00000590821.1:n.271+4452C>T
ENST00000590849.1:c.-52+4452C>T	ENSP00000467992.1:n.-52+4452C>T
ENST00000590980.1:c.-58+4452C>T	ENSP00000467472.1:n.-58+4452C>T
ENST00000592300.1:n.273-3679C>T
ENST00000592612.1:n.251-3682C>T
NM_002378.3:c.-58+4452C>T	NP_002369.2:n.-58+4452C>T
XM_011528019.1:c.-58+4452C>T	XP_011526321.1:n.-58+4452C>T
NM_002378.4:c.-58+4452C>T	NP_002369.2:n.-58+4452C>T