Canonical Allele Identifier: CA1594212897
Gene: ADAM19 HGNC NCBI

Linked Data

dbSNP Id: rs1756147542
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157518150A>T , CM000667.2:g.157518150A>T GRCh38
NC_000005.9:g.156945158A>T , CM000667.1:g.156945158A>T GRCh37
NC_000005.8:g.156877736A>T NCBI36
NG_046960.1:g.62674T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.666+673T>A MANE Select ENSP00000257527.5:n.666+673T>A
ENST00000257527.8:c.666+673T>A ENSP00000257527.4:n.666+673T>A
ENST00000517905.1:c.666+673T>A ENSP00000428654.1:n.666+673T>A
ENST00000517951.5:c.666+673T>A ENSP00000428376.1:n.666+673T>A
NM_033274.4:c.666+673T>A NP_150377.1:n.666+673T>A
XM_005266003.2:c.666+673T>A XP_005266060.1:n.666+673T>A
XM_011534680.1:c.-135-4645T>A XP_011532982.1:n.-135-4645T>A
XM_011534681.1:c.-145-4645T>A XP_011532983.1:n.-145-4645T>A
NM_033274.5:c.666+673T>A MANE Select NP_150377.1:n.666+673T>A
Search 100 bp 5'
Search 100 bp 3'