Canonical Allele Identifier: CA130185927

Gene: ADAM19

Linked Data

• dbSNP Id: rs937030356
• MyVariant Identifiers: chr5:g.156945231C>G (hg19) ; chr5:g.157518223C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157518223C>G , CM000667.2:g.157518223C>G	GRCh38
NC_000005.9:g.156945231C>G , CM000667.1:g.156945231C>G	GRCh37
NC_000005.8:g.156877809C>G	NCBI36
NG_046960.1:g.62601G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257527.9:c.666+600G>C MANE Select	ENSP00000257527.5:n.666+600G>C
ENST00000257527.8:c.666+600G>C	ENSP00000257527.4:n.666+600G>C
ENST00000517905.1:c.666+600G>C	ENSP00000428654.1:n.666+600G>C
ENST00000517951.5:c.666+600G>C	ENSP00000428376.1:n.666+600G>C
NM_033274.4:c.666+600G>C	NP_150377.1:n.666+600G>C
XM_005266003.2:c.666+600G>C	XP_005266060.1:n.666+600G>C
XM_011534680.1:c.-135-4718G>C	XP_011532982.1:n.-135-4718G>C
XM_011534681.1:c.-145-4718G>C	XP_011532983.1:n.-145-4718G>C
NM_033274.5:c.666+600G>C MANE Select	NP_150377.1:n.666+600G>C