Canonical Allele Identifier: CA363727959

Gene: SNRPC

Linked Data

• MyVariant Identifiers: chr6:g.34730405A>T (hg19) ; chr6:g.34762628A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34762628A>T , CM000668.2:g.34762628A>T	GRCh38
NC_000006.11:g.34730405A>T , CM000668.1:g.34730405A>T	GRCh37
NC_000006.10:g.34838383A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000244520.10:c.85A>T MANE Select	ENSP00000244520.5:p.Lys29Ter
ENST00000244520.9:c.85A>T	ENSP00000244520.5:p.Lys29Ter
ENST00000374017.3:c.148A>T	ENSP00000363129.3:p.Lys50Ter
ENST00000374018.5:c.-39A>T	ENSP00000363130.1:n.-39A>T
ENST00000474635.1:n.77A>T
NM_003093.2:c.85A>T	NP_003084.1:p.Lys29Ter
NR_029472.1:n.492A>T
NM_003093.3:c.85A>T MANE Select	NP_003084.1:p.Lys29Ter
NR_029472.2:n.81A>T