Canonical Allele Identifier: CA3432745

Linked Data

dbSNP Id: rs535005848

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.139273924C>T , CM000667.2:g.139273924C>T GRCh38
NC_000005.9:g.138609613C>T , CM000667.1:g.138609613C>T GRCh37
NC_000005.8:g.138637512C>T NCBI36
NG_012846.1:g.4822C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000506147.5:c.-256C>T ENSP00000423521.1:n.-256C>T
ENST00000508744.1:n.466-270G>A (SIL1)
ENST00000509400.5:n.293+6644G>A (SIL1)
ENST00000509990.5:c.-524C>T ENSP00000423533.1:n.-524C>T
ENST00000512107.5:c.-473C>T ENSP00000423695.1:n.-473C>T
NM_001194954.1:c.-524C>T (MATR3) NP_001181883.1:n.-524C>T
NM_001282278.1:c.-531C>T (MATR3) NP_001269207.1:n.-531C>T
NM_199189.2:c.-606C>T (MATR3) NP_954659.1:n.-606C>T
NR_003141.3:n.173C>T (SNHG4)
NR_036536.1:n.173C>T (SNHG4)